A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16039964



Internal ID2330182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31986254..31987899hg38UCSC Ensembl
Innerchr19:31986258..31987895hg38UCSC Ensembl
Outerchr19:31986250..31987903hg38UCSC Ensembl
chr19:32477160..32478805hg19UCSC Ensembl
Innerchr19:32477164..32478801hg19UCSC Ensembl
Outerchr19:32477156..32478809hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381646
hg191646
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644159
Supporting Variants
SamplesHG02073
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16039964
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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