A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342007



Internal ID20999560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:185214401..185229100hg38UCSC Ensembl
chr2:186079128..186093827hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3814700
hg1914700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4211n223
Supporting Variantsnssv18205359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342007
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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