A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575969



Internal ID16016692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72819272..72822354hg38UCSC Ensembl
Innerchr17:70815411..70818493hg19UCSC Ensembl
Innerchr17:68327006..68330088hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg383083
hg193083
hg183083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5764n54
Supporting Variantsnssv875960
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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