A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607515



Internal ID16394924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75731521..75758619hg38UCSC Ensembl
Innerchr7:75360839..75387937hg19UCSC Ensembl
Innerchr7:75198775..75225873hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3827099
hg1927099
hg1827099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1087864
Samples
Known GenesHIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607515
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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