A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575140



Internal ID16015863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45674547..45823708hg38UCSC Ensembl
Innerchr17:43751913..43901074hg19UCSC Ensembl
Innerchr17:41107696..41256855hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38149162
hg19149162
hg18149160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv872337
Samples
Known GenesCRHR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575140
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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