A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334295



Internal ID20867478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93926663..93926986hg38UCSC Ensembl
chr1:94392219..94392542hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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