A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15372784



Internal ID2324691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9697143..9700970hg38UCSC Ensembl
Innerchr16:9697170..9700943hg38UCSC Ensembl
Outerchr16:9697116..9700997hg38UCSC Ensembl
chr16:9791000..9794827hg19UCSC Ensembl
Innerchr16:9791027..9794800hg19UCSC Ensembl
Outerchr16:9790973..9794854hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg383828
hg193828
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637876
Supporting Variants
SamplesHG02070
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15372784
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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