A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15436863



Internal ID1200608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25814320..25824465hg38UCSC Ensembl
Innerchr16:25814328..25824457hg38UCSC Ensembl
Outerchr16:25814312..25824473hg38UCSC Ensembl
chr16:25825641..25835786hg19UCSC Ensembl
Innerchr16:25825649..25835778hg19UCSC Ensembl
Outerchr16:25825633..25835794hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3810146
hg1910146
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638282
Supporting Variants
SamplesHG01072
Known GenesHS3ST4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15436863
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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