A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644322



Internal ID7031078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39065435..39068983hg38UCSC Ensembl
Innerchr19:39065451..39068968hg38UCSC Ensembl
Outerchr19:39065420..39068999hg38UCSC Ensembl
chr19:39556075..39559623hg19UCSC Ensembl
Innerchr19:39556091..39559608hg19UCSC Ensembl
Outerchr19:39556060..39559639hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383549
hg193549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16054381
SamplesHG00148
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644322
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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