A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358431



Internal ID21015984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:168010101..168016900hg38UCSC Ensembl
chr3:167727889..167734688hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208591
Samples
Known GenesGOLIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358431
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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