A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639375



Internal ID6679469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82898377..82916482hg38UCSC Ensembl
Innerchr16:82898527..82916332hg38UCSC Ensembl
Outerchr16:82898227..82916632hg38UCSC Ensembl
chr16:82931982..82950087hg19UCSC Ensembl
Innerchr16:82932132..82949937hg19UCSC Ensembl
Outerchr16:82931832..82950237hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3818106
hg1918106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv545e214
Supporting Variantsessv15544593
SamplesHG01089
Known GenesCDH13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639375
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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