A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548268



Internal ID20921460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9822201..9824700hg38UCSC Ensembl
chr4_gl000193_random:89515..92014hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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