A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361019



Internal ID21018572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143568793..143571629hg38UCSC Ensembl
chr3:143287635..143290471hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382837
hg192837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094409
Samples
Known GenesSLC9A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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