A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv200n21



Internal ID20131921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16015985..16039969hg38UCSC Ensembl
chr19:16126795..16150779hg19UCSC Ensembl
chr19:15987795..16011779hg18UCSC Ensembl
chr19:15987795..16011779hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3823985
hg1923985
hg1823985
hg1723985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv517514, nsv524067
Samples
Known GenesLINC00661, LINC00905
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv200n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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