A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437449



Internal ID15382755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157808407..157809375hg38UCSC Ensembl
Outerchr4:157806587..157811424hg38UCSC Ensembl
Innerchr4:158729559..158730527hg19UCSC Ensembl
Outerchr4:158727739..158732576hg19UCSC Ensembl
Innerchr4:158949009..158949977hg18UCSC Ensembl
Outerchr4:158947189..158952026hg18UCSC Ensembl
Innerchr4:159307186..159308154hg16UCSC Ensembl
Outerchr4:159305366..159310203hg16UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg384838
hg194838
hg184838
hg164838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467330
SamplesNA18521
Known Genes
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv437449
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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