A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345702



Internal ID21003255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172668801..172706100hg38UCSC Ensembl
chr2:173533529..173570828hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3837300
hg1937300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345702
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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