A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366020



Internal ID21023573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113760464..113762304hg38UCSC Ensembl
chr3:113479311..113481151hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg381841
hg191841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207861
Samples
Known GenesATP6V1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366020
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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