A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15496312



Internal ID1689015
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638794
Supporting Variants
SamplesHG01566
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15496312
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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