A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400496



Internal ID21058049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119379308..119383751hg38UCSC Ensembl
chr5:118715003..118719446hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg384444
hg194444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212506
Samples
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400496
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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