A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072649



Internal ID15925835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:130683853..130794675hg38UCSC Ensembl
Innerchr6:131004998..131115817hg19UCSC Ensembl
Innerchr6:131046691..131157510hg18UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg38110823
hg19110820
hg18110820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604664
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1072649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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