A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15368124



Internal ID3182955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8034745..8053676hg38UCSC Ensembl
Innerchr16:8034771..8053651hg38UCSC Ensembl
Outerchr16:8034720..8053702hg38UCSC Ensembl
chr16:8084747..8103678hg19UCSC Ensembl
Innerchr16:8084773..8103653hg19UCSC Ensembl
Outerchr16:8084722..8103704hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3818932
hg1918932
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637818
Supporting Variants
SamplesHG02798
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15368124
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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