A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637876



Internal ID7024664
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15372783, essv15372784, essv15372785
SamplesHG02070, NA19776, HG00382
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637876
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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