A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035382



Internal ID19124601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19934474..19959156hg38UCSC Ensembl
Innerchr16:19945796..19970478hg19UCSC Ensembl
Innerchr16:19853297..19877979hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3824683
hg1924683
hg1824683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2791n100
Supporting Variantsnssv3546992, nssv3546991, nssv3546993
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035382
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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