A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15555212



Internal ID419799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87776388..87821346hg38UCSC Ensembl
Innerchr16:87776888..87820846hg38UCSC Ensembl
Outerchr16:87775388..87822346hg38UCSC Ensembl
chr16:87809994..87854952hg19UCSC Ensembl
Innerchr16:87810494..87854452hg19UCSC Ensembl
Outerchr16:87808994..87855952hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3844959
hg1944959
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639528
Supporting Variants
SamplesHG00127
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15555212
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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