A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638794



Internal ID7025579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62491182..62495954hg38UCSC Ensembl
chr16:62525086..62529858hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384773
hg194773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15496312
SamplesHG01566
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638794
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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