A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637869



Internal ID7024657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9218148..9219849hg38UCSC Ensembl
Innerchr16:9218198..9219799hg38UCSC Ensembl
Outerchr16:9218032..9219965hg38UCSC Ensembl
chr16:9312005..9313706hg19UCSC Ensembl
Innerchr16:9312055..9313656hg19UCSC Ensembl
Outerchr16:9311889..9313822hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381702
hg191702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15372773
SamplesHG02271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637869
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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