A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15990174



Internal ID6412167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9596338..9606033hg38UCSC Ensembl
Innerchr19:9596838..9605533hg38UCSC Ensembl
Outerchr19:9595338..9607033hg38UCSC Ensembl
chr19:9707014..9716709hg19UCSC Ensembl
Innerchr19:9707514..9716209hg19UCSC Ensembl
Outerchr19:9706014..9717709hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg389696
hg199696
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643636
Supporting Variants
SamplesNA20357
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15990174
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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