A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529673



Internal ID20903034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35751351..35756122hg38UCSC Ensembl
chr20:34339273..34344044hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg384772
hg194772
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529673
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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