A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688569



Internal ID15425221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81119963..81154273hg38UCSC Ensembl
Innerchr10:82879719..82914029hg19UCSC Ensembl
Innerchr10:82869699..82904009hg18UCSC Ensembl
Innerchr10:82869699..82904009hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3834311
hg1934311
hg1834311
hg1734311
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517526
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688569
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