A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638626



Internal ID7025411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52266481..52365522hg38UCSC Ensembl
chr16:52300393..52399434hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3899042
hg1999042
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15478275
SamplesHG02088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638626
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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