A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603266



Internal ID16043989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61471501..62189609hg38UCSC Ensembl
Innerchr6:61963172..62899514hg19UCSC Ensembl
Innerchr6:62021131..62957473hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38718109
hg19936343
hg18936343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1061075
Samples
Known GenesKHDRBS2, MTRNR2L9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603266
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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