A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074255



Internal ID15580755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145383210..145385191hg38UCSC Ensembl
Innerchr6:145704346..145706327hg19UCSC Ensembl
Innerchr6:145746039..145748020hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg381982
hg191982
hg181982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604825
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)nssv1074255
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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