A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644293



Internal ID7031049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37769130..37822111hg38UCSC Ensembl
Innerchr19:37769630..37821611hg38UCSC Ensembl
Outerchr19:37768130..37823111hg38UCSC Ensembl
chr19:38259770..38312751hg19UCSC Ensembl
Innerchr19:38260270..38312251hg19UCSC Ensembl
Outerchr19:38258770..38313751hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3852982
hg1952982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16051955
SamplesNA20785
Known GenesLOC644554, ZNF573
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644293
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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