A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603277



Internal ID16044000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61473996..62189609hg38UCSC Ensembl
Innerchr6:62183901..62899514hg19UCSC Ensembl
Innerchr6:62241860..62957473hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38715614
hg19715614
hg18715614
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051473
Samples
Known GenesKHDRBS2, MTRNR2L9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603277
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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