A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1070912



Internal ID15924098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102474767..102678952hg38UCSC Ensembl
Innerchr6:102922642..103126827hg19UCSC Ensembl
Innerchr6:103029335..103233520hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38204186
hg19204186
hg18204186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604327
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)nssv1070912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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