A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374426



Internal ID21031979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100330701..100337800hg38UCSC Ensembl
chr3:100049545..100056644hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208854
Samples
Known GenesNIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374426
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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