A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524058



Internal ID15104665
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699924
Samples
Known GenesADAMTS14, TBATA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524058
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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