A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6n21



Internal ID20131727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61813922..62052275hg38UCSC Ensembl
chr1:62279594..62517947hg19UCSC Ensembl
chr1:62052182..62290535hg18UCSC Ensembl
chr1:61991615..62229968hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38238354
hg19238354
hg18238354
hg17238354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522020, nsv518627
Samples
Known GenesINADL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv6n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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