A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv873555



Internal ID16167511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53238476..53572049hg38UCSC Ensembl
Innerchr17:51315837..51649410hg19UCSC Ensembl
Innerchr17:48670836..49004409hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38333574
hg19333574
hg18333574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575570
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)nssv873555
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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