A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539529



Internal ID20912824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12216301..12222200hg38UCSC Ensembl
chrUn_gl000235:20559..26473hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385900
hg195915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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