A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439586



Internal ID21097139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60522022..60527184hg38UCSC Ensembl
chr9_gl000199_random:3464..8626hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385163
hg195163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7753n223
Supporting Variantsnssv18227869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439586
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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