A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872206



Internal ID16166162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:44218858..44221066hg38UCSC Ensembl
Innerchr17:42296226..42298434hg19UCSC Ensembl
Innerchr17:39651752..39653960hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382209
hg192209
hg182209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575079
Supporting Variants
Samples
Known GenesUBTF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv872206
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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