A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204439



Internal ID20771479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:76702201..76726000hg38UCSC Ensembl
chr1:77167886..77191685hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3823800
hg1923800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328483
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204439
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00242


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