A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699924



Internal ID15089890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70757450..70779042hg38UCSC Ensembl
Innerchr10:72517206..72538798hg19UCSC Ensembl
Innerchr10:72187212..72208804hg18UCSC Ensembl
Innerchr10:72187212..72208804hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3821593
hg1921593
hg1821593
hg1721593
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524058
Supporting Variants
Samples
Known GenesADAMTS14, TBATA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699924
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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