A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15371998



Internal ID5373814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8743264..8764938hg38UCSC Ensembl
chr16:8837121..8858795hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3821675
hg1921675
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637844
Supporting Variants
SamplesHG01253
Known GenesABAT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15371998
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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