A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362414



Internal ID21019967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:175358501..175380200hg38UCSC Ensembl
chr3:175076290..175097989hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3821700
hg1921700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5100n223
Supporting Variantsnssv18211449
Samples
Known GenesMIR4789, NAALADL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362414
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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