A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644320



Internal ID7031076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39042497..39050323hg38UCSC Ensembl
Innerchr19:39042497..39050323hg38UCSC Ensembl
Outerchr19:39042321..39050511hg38UCSC Ensembl
chr19:39533137..39540963hg19UCSC Ensembl
Innerchr19:39533137..39540963hg19UCSC Ensembl
Outerchr19:39532961..39541151hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg387827
hg197827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16054377, essv16054376, essv16054378, essv16054379
SamplesNA19457, NA19327, NA19331, HG02095
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644320
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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