A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499910



Internal ID20873135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83152984..83345696hg38UCSC Ensembl
chr16:83186589..83379301hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38192713
hg19192713
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191013
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499910
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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