A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1070549



Internal ID15923735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99586704..99588097hg38UCSC Ensembl
Innerchr6:100034580..100035973hg19UCSC Ensembl
Innerchr6:100141301..100142694hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381394
hg191394
hg181394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604256
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)nssv1070549
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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