A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027703



Internal ID19116922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19063464..19089209hg38UCSC Ensembl
Innerchr8:18920974..18946719hg19UCSC Ensembl
Innerchr8:18965254..18990999hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3825746
hg1925746
hg1825746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760473
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)nsv1027703
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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