A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575583



Internal ID16362992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53501293..53572347hg38UCSC Ensembl
Innerchr17:51578654..51649708hg19UCSC Ensembl
Innerchr17:48933653..49004707hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3871055
hg1971055
hg1871055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5696n54
Supporting Variantsnssv873567
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575583
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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