A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522098



Internal ID15449391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37564327..37578147hg38UCSC Ensembl
Innerchr6:37532103..37545923hg19UCSC Ensembl
Innerchr6:37640081..37653901hg18UCSC Ensembl
Innerchr6:37640081..37653901hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3813821
hg1913821
hg1813821
hg1713821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv381n21
Supporting Variantsnssv694870
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522098
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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