A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012443



Internal ID19101660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41317573..41782940hg38UCSC Ensembl
Innerchr3:41359064..41824432hg19UCSC Ensembl
Innerchr3:41334068..41799436hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38465368
hg19465369
hg18465369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4723n100
Supporting Variantsnssv3589708, nssv3589706, nssv3739707, nssv3589707
Samples
Known GenesULK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012443
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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