A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030398



Internal ID19119617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54193220..54266331hg38UCSC Ensembl
Innerchr7:54260913..54334024hg19UCSC Ensembl
Innerchr7:54228407..54301518hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3873112
hg1973112
hg1873112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661322
Samples
Known GenesHPVC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030398
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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