A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517890



Internal ID15445183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153238742..153248452hg38UCSC Ensembl
Innerchr6:153559877..153569587hg19UCSC Ensembl
Innerchr6:153601570..153611280hg18UCSC Ensembl
Innerchr6:153651991..153661701hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg389711
hg199711
hg189711
hg179711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695298
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517890
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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