A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638873



Internal ID7025658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66871717..66876903hg38UCSC Ensembl
Innerchr16:66871739..66876881hg38UCSC Ensembl
Outerchr16:66871695..66876925hg38UCSC Ensembl
chr16:66905620..66910806hg19UCSC Ensembl
Innerchr16:66905642..66910784hg19UCSC Ensembl
Outerchr16:66905598..66910828hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg385187
hg195187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501376
SamplesHG01537
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638873
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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