A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012561



Internal ID19101778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21053677..21200164hg38UCSC Ensembl
Innerchr3:21095169..21241656hg19UCSC Ensembl
Innerchr3:21070173..21216660hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38146488
hg19146488
hg18146488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4688n100
Supporting Variantsnssv3593106
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)nsv1012561
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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