A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372377



Internal ID21029930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172933801..172934900hg38UCSC Ensembl
chr3:172651591..172652690hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098225
Samples
Known GenesSPATA16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372377
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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