A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029085



Internal ID19118304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20291660..20324132hg38UCSC Ensembl
Innerchr7:20331283..20363755hg19UCSC Ensembl
Innerchr7:20297808..20330280hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3832473
hg1932473
hg1832473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643267
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)nsv1029085
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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