A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437822



Internal ID15383128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14939394..14946139hg38UCSC Ensembl
Outerchr18:14938840..14947954hg38UCSC Ensembl
Innerchr18:14939393..14946138hg19UCSC Ensembl
Outerchr18:14938839..14947953hg19UCSC Ensembl
Innerchr18:14929393..14936138hg18UCSC Ensembl
Outerchr18:14928839..14937953hg18UCSC Ensembl
Innerchr18:14927388..14934133hg16UCSC Ensembl
Outerchr18:14926834..14935948hg16UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg389115
hg199115
hg189115
hg169115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467703
SamplesNA18854
Known GenesLOC400644
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)nsv437822
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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