A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023616



Internal ID18766149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14305285..15546754hg38UCSC Ensembl
Innerchr7:14344910..15586379hg19UCSC Ensembl
Innerchr7:14311435..15552904hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381241470
hg191241470
hg181241470
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752897
Samples
Known GenesAGMO, DGKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023616
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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