A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705654



Internal ID15442306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11894591..11895538hg38UCSC Ensembl
Innerchr10:11936590..11937537hg19UCSC Ensembl
Innerchr10:11976596..11977543hg18UCSC Ensembl
Innerchr10:11976596..11977543hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38948
hg19948
hg18948
hg17948
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528958
Supporting Variants
Samples
Known GenesPROSER2-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705654
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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