A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv381n21



Internal ID22766573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37564327..37578147hg38UCSC Ensembl
chr6:37532103..37545923hg19UCSC Ensembl
chr6:37640081..37653901hg18UCSC Ensembl
chr6:37640081..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 Variants
Supporting Variantsnsv522466, nsv522098
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv381n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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