A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575139



Internal ID16362548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45674547..45771129hg38UCSC Ensembl
Innerchr17:43751913..43848495hg19UCSC Ensembl
Innerchr17:41107696..41204264hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3896583
hg1996583
hg1896569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv872336
Samples
Known GenesCRHR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575139
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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