A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000508



Internal ID19089725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41648586..41800258hg38UCSC Ensembl
Innerchr3:41690077..41841750hg19UCSC Ensembl
Innerchr3:41665081..41816754hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38151673
hg19151674
hg18151674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739708
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)nsv1000508
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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