A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639601



Internal ID6679692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89845985..89862110hg38UCSC Ensembl
Innerchr16:89846019..89862077hg38UCSC Ensembl
Outerchr16:89845952..89862144hg38UCSC Ensembl
chr16:89912393..89928518hg19UCSC Ensembl
Innerchr16:89912427..89928485hg19UCSC Ensembl
Outerchr16:89912360..89928552hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3816126
hg1916126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15569955
SamplesHG02221
Known GenesSPIRE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639601
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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