A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637932



Internal ID7024719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11665902..11667607hg38UCSC Ensembl
Innerchr16:11665915..11667595hg38UCSC Ensembl
Outerchr16:11665890..11667620hg38UCSC Ensembl
chr16:11759758..11761463hg19UCSC Ensembl
Innerchr16:11759771..11761451hg19UCSC Ensembl
Outerchr16:11759746..11761476hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381706
hg191706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377007, essv15377008, essv15377009, essv15377006
SamplesHG03267, NA18915, NA19019, NA19380
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637932
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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