A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704276



Internal ID15440928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133344451..133402966hg38UCSC Ensembl
Innerchr10:135157955..135216470hg19UCSC Ensembl
Innerchr10:135007945..135066460hg18UCSC Ensembl
Innerchr10:135046836..135105351hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3858516
hg1958516
hg1858516
hg1758516
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527785
Supporting Variants
Samples
Known GenesECHS1, FUOM, MIR3944, MTG1, PAOX, PRAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704276
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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