A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644182



Internal ID6684250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33159502..33164577hg38UCSC Ensembl
Innerchr19:33159502..33164577hg38UCSC Ensembl
Outerchr19:33159002..33165077hg38UCSC Ensembl
chr19:33650408..33655483hg19UCSC Ensembl
Innerchr19:33650408..33655483hg19UCSC Ensembl
Outerchr19:33649908..33655983hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg385076
hg195076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16041344, essv16041345
SamplesNA18639, HG00699
Known GenesWDR88
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644182
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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