A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638279



Internal ID6678377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25681236..25692538hg38UCSC Ensembl
Innerchr16:25681386..25692388hg38UCSC Ensembl
Outerchr16:25681086..25692688hg38UCSC Ensembl
chr16:25692557..25703859hg19UCSC Ensembl
Innerchr16:25692707..25703709hg19UCSC Ensembl
Outerchr16:25692407..25704009hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3811303
hg1911303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15434572
SamplesHG00419
Known GenesHS3ST4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638279
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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