A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15968190



Internal ID632151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1950306..1951854hg38UCSC Ensembl
Innerchr19:1950329..1951832hg38UCSC Ensembl
Outerchr19:1950284..1951877hg38UCSC Ensembl
chr19:1950305..1951853hg19UCSC Ensembl
Innerchr19:1950328..1951831hg19UCSC Ensembl
Outerchr19:1950283..1951876hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381549
hg191549
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643415
Supporting Variants
SamplesHG00276
Known GenesCSNK1G2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15968190
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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