A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15997548



Internal ID3362561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14810861..14811696hg38UCSC Ensembl
Innerchr19:14810862..14811695hg38UCSC Ensembl
Outerchr19:14810860..14811697hg38UCSC Ensembl
chr19:14921673..14922508hg19UCSC Ensembl
Innerchr19:14921674..14922507hg19UCSC Ensembl
Outerchr19:14921672..14922509hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643753
Supporting Variants
SamplesHG03015
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15997548
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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