A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638073



Internal ID6678171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:17264060..17266980hg38UCSC Ensembl
Innerchr16:17264065..17266975hg38UCSC Ensembl
Outerchr16:17264055..17266985hg38UCSC Ensembl
chr16:17357917..17360837hg19UCSC Ensembl
Innerchr16:17357922..17360832hg19UCSC Ensembl
Outerchr16:17357912..17360842hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg382921
hg192921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15390669
SamplesHG03063
Known GenesXYLT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638073
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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