A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326159



Internal ID20859293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37963926..37966994hg38UCSC Ensembl
chr1:38429598..38432666hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383069
hg193069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061217
Samples
Known GenesSF3A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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