A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638619



Internal ID7025404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51911236..51912329hg38UCSC Ensembl
Innerchr16:51911286..51912279hg38UCSC Ensembl
Outerchr16:51911179..51912386hg38UCSC Ensembl
chr16:51945148..51946241hg19UCSC Ensembl
Innerchr16:51945198..51946191hg19UCSC Ensembl
Outerchr16:51945091..51946298hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg381094
hg191094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15478207
SamplesHG03052
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638619
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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