A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604054



Internal ID16391463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80523276..80577958hg38UCSC Ensembl
Innerchr6:81232993..81287675hg19UCSC Ensembl
Innerchr6:81289712..81344394hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3854683
hg1954683
hg1854683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154811
Samples1780854158_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604054
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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