A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994852



Internal ID6730802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9610195..9615304hg38UCSC Ensembl
Outerchr19:9720871..9725980hg19UCSC Ensembl
Outerchr19:9581871..9586980hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383208
hg193208
hg183208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565404
SamplesHuRef
Known GenesZNF561
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994852
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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