A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638927



Internal ID7025712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69541021..69543908hg38UCSC Ensembl
Innerchr16:69541037..69543893hg38UCSC Ensembl
Outerchr16:69541006..69543924hg38UCSC Ensembl
chr16:69574924..69577811hg19UCSC Ensembl
Innerchr16:69574940..69577796hg19UCSC Ensembl
Outerchr16:69574909..69577827hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382888
hg192888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15503739, essv15503744, essv15503737, essv15503743, essv15503740, essv15503742, essv15503738, essv15503741
SamplesHG03722, HG03986, HG03744, HG03974, HG03846, HG03973, HG03863, HG01583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638927
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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