A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604389



Internal ID16391798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104106806..104191244hg38UCSC Ensembl
Innerchr6:104554681..104639119hg19UCSC Ensembl
Innerchr6:104661374..104745812hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3884439
hg1984439
hg1884439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071655
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604389
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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