A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15371979



Internal ID5373795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8732186..8733864hg38UCSC Ensembl
Innerchr16:8732187..8733863hg38UCSC Ensembl
Outerchr16:8732185..8733865hg38UCSC Ensembl
chr16:8826043..8827721hg19UCSC Ensembl
Innerchr16:8826044..8827720hg19UCSC Ensembl
Outerchr16:8826042..8827722hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381679
hg191679
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637843
Supporting Variants
SamplesNA19189
Known GenesABAT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15371979
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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