A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696486



Internal ID15433138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11131547..11137550hg38UCSC Ensembl
Innerchr8:10989057..10995060hg19UCSC Ensembl
Innerchr8:11026467..11032470hg18UCSC Ensembl
Innerchr8:11026467..11032470hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386004
hg196004
hg186004
hg176004
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516033
Supporting Variants
Samples
Known GenesXKR6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696486
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