A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639545



Internal ID7026325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88291388..88293411hg38UCSC Ensembl
Innerchr16:88291394..88293406hg38UCSC Ensembl
Outerchr16:88291383..88293417hg38UCSC Ensembl
chr16:88324994..88327017hg19UCSC Ensembl
Innerchr16:88325000..88327012hg19UCSC Ensembl
Outerchr16:88324989..88327023hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382024
hg192024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15563490
SamplesHG03717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639545
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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