A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639374



Internal ID6679468
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv545e214
Supporting Variantsessv15544591, essv15544590, essv15544592
SamplesHG01275, HG01344, HG01089
Known GenesCDH13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639374
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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