A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868983



Internal ID16162939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27164439..27210955hg38UCSC Ensembl
Innerchr17:25491465..25537981hg19UCSC Ensembl
Innerchr17:22515592..22562108hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3846517
hg1946517
hg1846517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574641
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868983
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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