A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491901



Internal ID21149454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35100202..35178928hg38UCSC Ensembl
chr14:35569408..35648134hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3878727
hg1978727
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191648
Samples
Known GenesKIAA0391, PPP2R3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491901
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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