A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1071901



Internal ID15925087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107114554..107115608hg38UCSC Ensembl
Innerchr6:107435758..107436812hg19UCSC Ensembl
Innerchr6:107542451..107543505hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381055
hg191055
hg181055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604449
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)nssv1071901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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