A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15554038



Internal ID820983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87146356..87165128hg38UCSC Ensembl
Innerchr16:87146394..87165091hg38UCSC Ensembl
Outerchr16:87146319..87165166hg38UCSC Ensembl
chr16:87179962..87198734hg19UCSC Ensembl
Innerchr16:87180000..87198697hg19UCSC Ensembl
Outerchr16:87179925..87198772hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3818773
hg1918773
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639502
Supporting Variants
SamplesHG00407
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15554038
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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