A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16002822



Internal ID6004638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16693655..16706615hg38UCSC Ensembl
Innerchr19:16694155..16706115hg38UCSC Ensembl
Outerchr19:16692655..16707615hg38UCSC Ensembl
chr19:16804466..16817426hg19UCSC Ensembl
Innerchr19:16804966..16816926hg19UCSC Ensembl
Outerchr19:16803466..16818426hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3812961
hg1912961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643800
Supporting Variants
SamplesNA19917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16002822
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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