A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638795



Internal ID7025580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62491182..62495954hg38UCSC Ensembl
chr16:62525086..62529858hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384773
hg194773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15496314, essv15496313
SamplesNA19795, HG00554
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638795
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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