A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869632



Internal ID16163588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33283169..33293011hg38UCSC Ensembl
Innerchr17:31610187..31620029hg19UCSC Ensembl
Innerchr17:28634300..28644142hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg389843
hg199843
hg189843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574711
Supporting Variants
Samples
Known GenesASIC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869632
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