A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700809



Internal ID15090775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:83680371..83684024hg38UCSC Ensembl
Innerchr15:84349123..84352776hg19UCSC Ensembl
Innerchr15:82140127..82143780hg18UCSC Ensembl
Innerchr15:82140127..82143780hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg383654
hg193654
hg183654
hg173654
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524815
Supporting Variants
Samples
Known GenesADAMTSL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700809
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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