A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15990795



Internal ID5992611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11523953..11528541hg38UCSC Ensembl
Innerchr19:11524006..11528488hg38UCSC Ensembl
Outerchr19:11523900..11528594hg38UCSC Ensembl
chr19:11634768..11639356hg19UCSC Ensembl
Innerchr19:11634821..11639303hg19UCSC Ensembl
Outerchr19:11634715..11639409hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384589
hg194589
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643673
Supporting Variants
SamplesHG02006
Known GenesECSIT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15990795
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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