A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639060



Internal ID7025844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74315642..74364792hg38UCSC Ensembl
Innerchr16:74316142..74364292hg38UCSC Ensembl
Outerchr16:74314642..74365792hg38UCSC Ensembl
chr16:74349540..74398690hg19UCSC Ensembl
Innerchr16:74350040..74398190hg19UCSC Ensembl
Outerchr16:74348540..74399690hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3849151
hg1949151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15516733
SamplesHG03511
Known GenesLOC283922
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639060
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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