A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004603



Internal ID19093820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51856772..52038525hg38UCSC Ensembl
Innerchr2:52083910..52265663hg19UCSC Ensembl
Innerchr2:51937414..52119167hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38181754
hg19181754
hg18181754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3816n100
Supporting Variantsnssv3726027
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)nsv1004603
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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