A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654045



Internal ID15390697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120909696..120917947hg38UCSC Ensembl
Innerchr10:122669208..122677459hg19UCSC Ensembl
Innerchr10:122659198..122667449hg18UCSC Ensembl
Innerchr10:122659198..122667449hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg388252
hg198252
hg188252
hg178252
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517219
Supporting Variants
Samples
Known GenesMIR5694
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654045
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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