A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv202n21



Internal ID20131923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39353536..39359462hg38UCSC Ensembl
chr19:39844176..39850102hg19UCSC Ensembl
chr19:44536016..44541942hg18UCSC Ensembl
chr19:44536016..44541942hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385927
hg195927
hg185927
hg175927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520245, nsv526707
Samples
Known GenesSAMD4B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv202n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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