A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15503741



Internal ID4307338
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638927
Supporting Variants
SamplesHG03863
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15503741
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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