A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16039963



Internal ID2330178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31973874..31984373hg38UCSC Ensembl
Innerchr19:31973874..31984373hg38UCSC Ensembl
Outerchr19:31973374..31984873hg38UCSC Ensembl
chr19:32464780..32475279hg19UCSC Ensembl
Innerchr19:32464780..32475279hg19UCSC Ensembl
Outerchr19:32464280..32475779hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3810500
hg1910500
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644158
Supporting Variants
SamplesHG02073
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16039963
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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