A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637983



Internal ID7024769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13414831..13415618hg38UCSC Ensembl
Innerchr16:13414831..13415618hg38UCSC Ensembl
Outerchr16:13414635..13415773hg38UCSC Ensembl
chr16:13508688..13509475hg19UCSC Ensembl
Innerchr16:13508688..13509475hg19UCSC Ensembl
Outerchr16:13508492..13509630hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15378558
SamplesNA18539
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637983
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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