A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15375221



Internal ID6212513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11205696..11208613hg38UCSC Ensembl
Innerchr16:11205696..11208613hg38UCSC Ensembl
Outerchr16:11205507..11208777hg38UCSC Ensembl
chr16:11299553..11302470hg19UCSC Ensembl
Innerchr16:11299553..11302470hg19UCSC Ensembl
Outerchr16:11299364..11302634hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382918
hg192918
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637923
Supporting Variants
SamplesNA19740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15375221
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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