A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575690



Internal ID16016413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:55887196..55947396hg38UCSC Ensembl
Innerchr17:53964557..54024757hg19UCSC Ensembl
Innerchr17:51319556..51379756hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3860201
hg1960201
hg1860201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv874123
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575690
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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