A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1060908



Internal ID15914094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:55961339..56002991hg38UCSC Ensembl
Innerchr6:55826137..55867789hg19UCSC Ensembl
Innerchr6:55934096..55975748hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3841653
hg1941653
hg1841653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603176
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)nssv1060908
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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