A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603641



Internal ID16391050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:72142085..72158242hg38UCSC Ensembl
Innerchr6:72851788..72867945hg19UCSC Ensembl
Innerchr6:72908509..72924666hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3816158
hg1916158
hg1816158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1063667
Samples
Known GenesRIMS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603641
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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