A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348370



Internal ID21005923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143917001..143945300hg38UCSC Ensembl
chr2:144674568..144702867hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3828300
hg1928300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4146n223
Supporting Variantsnssv18207293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348370
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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