A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328640



Internal ID20861788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23765143..23767333hg38UCSC Ensembl
chr1:24091633..24093823hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382191
hg192191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202495
Samples
Known GenesLOC100506963
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328640
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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