A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016508



Internal ID19105727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:68703840..68726277hg38UCSC Ensembl
Innerchr7:68168827..68191264hg19UCSC Ensembl
Innerchr7:67806763..67829200hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3822438
hg1922438
hg1822438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655636
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)nsv1016508
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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