A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639332



Internal ID7026115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81412855..81442861hg38UCSC Ensembl
Innerchr16:81412855..81442861hg38UCSC Ensembl
Outerchr16:81412355..81443361hg38UCSC Ensembl
chr16:81446460..81476466hg19UCSC Ensembl
Innerchr16:81446460..81476466hg19UCSC Ensembl
Outerchr16:81445960..81476966hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3830007
hg1930007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15537855, essv15537854
SamplesHG02661, HG02554
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639332
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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