A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518432



Internal ID15099039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100458543..100467096hg38UCSC Ensembl
Innerchr7:100056166..100064719hg19UCSC Ensembl
Innerchr7:99894102..99902655hg18UCSC Ensembl
Innerchr7:99700817..99709370hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg388554
hg198554
hg188554
hg178554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695866
Samples
Known GenesC7orf61, TSC22D4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518432
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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