A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637667



Internal ID7024457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3442554..3448680hg38UCSC Ensembl
chr16:3492554..3498680hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386127
hg196127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363071
SamplesNA07037
Known GenesNAA60, ZNF597
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637667
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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