A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv396n21



Internal ID22766588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141752887..141808872hg38UCSC Ensembl
chr6:142074024..142130009hg19UCSC Ensembl
chr6:142115717..142171702hg18UCSC Ensembl
chr6:142115717..142171702hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3855986
hg1955986
hg1855986
hg1755986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv525384, nsv523425
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv396n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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