A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698810



Internal ID15088776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72738548..72739848hg38UCSC Ensembl
Innerchr17:70734687..70735987hg19UCSC Ensembl
Innerchr17:68246282..68247582hg18UCSC Ensembl
Innerchr17:68246282..68247582hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381301
hg191301
hg181301
hg171301
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519333
Supporting Variants
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698810
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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