A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872431



Internal ID15819701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46172472..46192809hg38UCSC Ensembl
Innerchr17:44249838..44270175hg19UCSC Ensembl
Innerchr17:41605615..41625952hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3820338
hg1920338
hg1820338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575192
Supporting Variants
Samples
Known GenesKANSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv872431
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer