A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15377085



Internal ID6041523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11820541..11822201hg38UCSC Ensembl
Innerchr16:11820592..11822151hg38UCSC Ensembl
Outerchr16:11820491..11822252hg38UCSC Ensembl
chr16:11914398..11916058hg19UCSC Ensembl
Innerchr16:11914449..11916008hg19UCSC Ensembl
Outerchr16:11914348..11916109hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381661
hg191661
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637941
Supporting Variants
SamplesNA19443
Known GenesBCAR4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15377085
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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