A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600983



Internal ID16041706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10469593..10527985hg38UCSC Ensembl
Innerchr6:10469826..10528218hg19UCSC Ensembl
Innerchr6:10577812..10636204hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3858393
hg1958393
hg1858393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10300n54
Supporting Variantsnssv1049402
Samples
Known GenesGCNT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600983
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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