A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333296



Internal ID20866472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153549090..153549894hg38UCSC Ensembl
chr1:153521566..153522370hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200474
Samples
Known GenesS100A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333296
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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