A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15377008



Internal ID5572633
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637932
Supporting Variants
SamplesNA19019
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15377008
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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