A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643422



Internal ID6683496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2314254..2337163hg38UCSC Ensembl
chr19:2314253..2337162hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3822910
hg1922910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15969539
SamplesHG03246
Known GenesLSM7, SPPL2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643422
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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