A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604249



Internal ID16391658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:97680078..97725104hg38UCSC Ensembl
Innerchr6:98127954..98172980hg19UCSC Ensembl
Innerchr6:98234675..98279701hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3845027
hg1945027
hg1845027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154853
SamplesHGDP00870
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604249
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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