A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637923



Internal ID7024710
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15375224, essv15375223, essv15375222, essv15375221
SamplesNA20910, NA20587, NA20533, NA19740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637923
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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