A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526019



Internal ID15453312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25566500..25575601hg38UCSC Ensembl
Innerchr7:25606120..25615221hg19UCSC Ensembl
Innerchr7:25572645..25581746hg18UCSC Ensembl
Innerchr7:25379360..25388461hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg389102
hg199102
hg189102
hg179102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv417n21
Supporting Variantsnssv702249
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526019
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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