A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604258



Internal ID16391667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99792391..99841750hg38UCSC Ensembl
Innerchr6:100240267..100289626hg19UCSC Ensembl
Innerchr6:100346988..100396347hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3849360
hg1949360
hg1849360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1070554
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604258
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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