A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575964



Internal ID16016687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72819082..72821975hg38UCSC Ensembl
Innerchr17:70815221..70818114hg19UCSC Ensembl
Innerchr17:68326816..68329709hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg382894
hg192894
hg182894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5764n54
Supporting Variantsnssv875941
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575964
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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