A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643474



Internal ID7030236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3789997..3791438hg38UCSC Ensembl
Innerchr19:3789997..3791438hg38UCSC Ensembl
Outerchr19:3789659..3791603hg38UCSC Ensembl
chr19:3789995..3791436hg19UCSC Ensembl
Innerchr19:3789995..3791436hg19UCSC Ensembl
Outerchr19:3789657..3791601hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381442
hg191442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15977382, essv15977383, essv15977384, essv15977385
SamplesNA12383, NA20517, NA20795, HG00149
Known GenesMATK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643474
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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