A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643857



Internal ID7030614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19758916..19762083hg38UCSC Ensembl
Innerchr19:19758966..19762033hg38UCSC Ensembl
Outerchr19:19758866..19762133hg38UCSC Ensembl
chr19:19869725..19872892hg19UCSC Ensembl
Innerchr19:19869775..19872842hg19UCSC Ensembl
Outerchr19:19869675..19872942hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383168
hg193168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16006927
SamplesHG03515
Known GenesLINC00663
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643857
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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