A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637844



Internal ID6677944
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15371999, essv15371998, essv15371997
SamplesHG01492, HG01253, HG00531
Known GenesABAT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637844
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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