A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371247



Internal ID21028800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:175359369..175369891hg38UCSC Ensembl
chr3:175077158..175087680hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3810523
hg1910523
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211450
Samples
Known GenesMIR4789, NAALADL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371247
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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