A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869005



Internal ID16162961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27643821..27745423hg38UCSC Ensembl
Innerchr17:25970847..26072449hg19UCSC Ensembl
Innerchr17:22994974..23096576hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38101603
hg19101603
hg18101603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574651
Supporting Variants
Samples
Known GenesLGALS9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869005
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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