A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739708



Internal ID19037989
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 StatusS
Merged Variantsnsv1000508
Supporting Variants
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)nssv3739708
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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