A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575963



Internal ID16363372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72807479..72823904hg38UCSC Ensembl
Innerchr17:70803618..70820043hg19UCSC Ensembl
Innerchr17:68315213..68331638hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3816426
hg1916426
hg1816426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5763n54
Supporting Variantsnssv875940
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575963
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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