A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437402



Internal ID15382708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:12164627..12164897hg38UCSC Ensembl
Outerchr2:12160905..12167822hg38UCSC Ensembl
Innerchr2:12304753..12305023hg19UCSC Ensembl
Outerchr2:12301031..12307948hg19UCSC Ensembl
Innerchr2:12222204..12222474hg18UCSC Ensembl
Outerchr2:12218482..12225399hg18UCSC Ensembl
Innerchr2:12326492..12326762hg16UCSC Ensembl
Outerchr2:12322770..12329687hg16UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg386918
hg196918
hg186918
hg166918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467283
SamplesNA12801
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)nsv437402
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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