A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3493724



Internal ID19081365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:216981772..217033423hg38UCSC Ensembl
Innerchr1:217155114..217206765hg19UCSC Ensembl
Innerchr1:215221737..215273388hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3851652
hg1951652
hg1851652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008670
Supporting Variants
Samples
Known GenesESRRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3493724
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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