A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1067631



Internal ID15574131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:87107187..87196335hg38UCSC Ensembl
Innerchr6:87816905..87906053hg19UCSC Ensembl
Innerchr6:87873624..87962772hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3889149
hg1989149
hg1889149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604114
Supporting Variants
Samples
Known GenesZNF292
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1067631
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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