A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021056



Internal ID18763590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14122900..14229818hg38UCSC Ensembl
Innerchr7:14162525..14269443hg19UCSC Ensembl
Innerchr7:14129050..14235968hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38106919
hg19106919
hg18106919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643153
Samples
Known GenesDGKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021056
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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