A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643760



Internal ID6683830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15050284..15092172hg38UCSC Ensembl
Innerchr19:15050434..15092022hg38UCSC Ensembl
Outerchr19:15050134..15092322hg38UCSC Ensembl
chr19:15161095..15202983hg19UCSC Ensembl
Innerchr19:15161245..15202833hg19UCSC Ensembl
Outerchr19:15160945..15203133hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3841889
hg1941889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv654e214
Supporting Variantsessv15999919, essv15999920
SamplesHG01046, HG00182
Known GenesCASP14, OR1I1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643760
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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