A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013763



Internal ID18756295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:239192855..239401382hg38UCSC Ensembl
Innerchr1:239356155..239564682hg19UCSC Ensembl
Innerchr1:237422778..237631305hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38208528
hg19208528
hg18208528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv594n100
Supporting Variantsnssv3705545
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)nsv1013763
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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