A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644238



Internal ID6684306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35527148..35528844hg38UCSC Ensembl
Innerchr19:35527148..35528844hg38UCSC Ensembl
Outerchr19:35527025..35529038hg38UCSC Ensembl
chr19:36018050..36019746hg19UCSC Ensembl
Innerchr19:36018050..36019746hg19UCSC Ensembl
Outerchr19:36017927..36019940hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381697
hg191697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16046262
SamplesNA18916
Known GenesSBSN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644238
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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