A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv873558



Internal ID16167514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53380381..53535874hg38UCSC Ensembl
Innerchr17:51457742..51613235hg19UCSC Ensembl
Innerchr17:48812741..48968234hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38155494
hg19155494
hg18155494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575574
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)nssv873558
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