A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023584



Internal ID21932927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67280903..67348528hg38UCSC Ensembl
chr14:67747620..67815245hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3867626
hg1967626
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600732
Samples
Known GenesATP6V1D, MPP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023584
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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