A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604256



Internal ID16391665
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 StatusM
Merged Variants
Supporting Variantsnssv1070549
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604256
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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