A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637677



Internal ID7024467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3922940..3931101hg38UCSC Ensembl
Innerchr16:3922944..3931098hg38UCSC Ensembl
Outerchr16:3922937..3931105hg38UCSC Ensembl
chr16:3972941..3981102hg19UCSC Ensembl
Innerchr16:3972945..3981099hg19UCSC Ensembl
Outerchr16:3972938..3981106hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388162
hg198162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363308, essv15363307, essv15363306
SamplesHG00277, HG00324, HG00276
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637677
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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