A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575986



Internal ID16016709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72983699..72984275hg38UCSC Ensembl
Innerchr17:70979838..70980414hg19UCSC Ensembl
Innerchr17:68491433..68492009hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38577
hg19577
hg18577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876057
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575986
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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