A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15544590



Internal ID5546406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82895839..82919754hg38UCSC Ensembl
chr16:82929444..82953359hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3823916
hg1923916
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639374
Supporting Variants
SamplesHG01089
Known GenesCDH13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15544590
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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