A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575137



Internal ID16362546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45603938..45627130hg38UCSC Ensembl
Innerchr17:43681304..43704496hg19UCSC Ensembl
Innerchr17:41037087..41060279hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3823193
hg1923193
hg1823193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv872335
Samples
Known GenesCRHR1, MGC57346
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575137
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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