A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639411



Internal ID7026192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84091200..84098482hg38UCSC Ensembl
Innerchr16:84091209..84098474hg38UCSC Ensembl
Outerchr16:84091192..84098491hg38UCSC Ensembl
chr16:84124805..84132087hg19UCSC Ensembl
Innerchr16:84124814..84132079hg19UCSC Ensembl
Outerchr16:84124797..84132096hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg387283
hg197283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15545795
SamplesNA18995
Known GenesMBTPS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639411
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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