A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515696



Internal ID15443307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75731521..75739895hg38UCSC Ensembl
Innerchr7:75360839..75369213hg19UCSC Ensembl
Innerchr7:75198775..75207149hg18UCSC Ensembl
Innerchr7:75005490..75013864hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg388375
hg198375
hg188375
hg178375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699828, nssv651998, nssv704636, nssv686150, nssv660530, nssv659459
Samples
Known GenesHIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515696
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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