A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639394



Internal ID6679488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83757997..83779655hg38UCSC Ensembl
Innerchr16:83757997..83779655hg38UCSC Ensembl
Outerchr16:83757497..83780155hg38UCSC Ensembl
chr16:83791602..83813260hg19UCSC Ensembl
Innerchr16:83791602..83813260hg19UCSC Ensembl
Outerchr16:83791102..83813760hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3821659
hg1921659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15545356
SamplesNA19786
Known GenesCDH13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639394
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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