A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639253



Internal ID7026036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79890636..79936424hg38UCSC Ensembl
Innerchr16:79890636..79936424hg38UCSC Ensembl
Outerchr16:79890136..79936924hg38UCSC Ensembl
chr16:79924533..79970321hg19UCSC Ensembl
Innerchr16:79924533..79970321hg19UCSC Ensembl
Outerchr16:79924033..79970821hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3845789
hg1945789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15532507
SamplesNA20778
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639253
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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