A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694432



Internal ID15431084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6252841..6253585hg38UCSC Ensembl
Innerchr10:6294804..6295548hg19UCSC Ensembl
Innerchr10:6334810..6335554hg18UCSC Ensembl
Innerchr10:6334810..6335554hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38745
hg19745
hg18745
hg17745
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521313
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694432
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer