A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644857



Internal ID7031608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56115417..56116556hg38UCSC Ensembl
Innerchr19:56115456..56116518hg38UCSC Ensembl
Outerchr19:56115379..56116595hg38UCSC Ensembl
chr19:56626786..56627925hg19UCSC Ensembl
Innerchr19:56626825..56627887hg19UCSC Ensembl
Outerchr19:56626748..56627964hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16100869, essv16100870
SamplesHG03045, HG02760
Known GenesZNF787
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644857
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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