A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv206n21



Internal ID20131927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56026162..56195679hg38UCSC Ensembl
chr19:56537528..56707048hg19UCSC Ensembl
chr19:61229340..61398860hg18UCSC Ensembl
chr19:61229340..61398860hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38169518
hg19169521
hg18169521
hg17169521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528998, nsv523651
Samples
Known GenesGALP, NLRP5, ZNF444, ZNF787, ZSCAN5B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv206n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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