A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586822



Internal ID6711518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50875749..50876454hg38UCSC Ensembl
Innerchr19:51379005..51379710hg19UCSC Ensembl
Innerchr19:56070817..56071522hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38706
hg19706
hg18706
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1010987
Supporting Variants
SamplesHuRef
Known GenesKLK2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586822
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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