A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366842



Internal ID21024395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143619495..143621364hg38UCSC Ensembl
chr3:143338337..143340206hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381870
hg191870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094412
Samples
Known GenesSLC9A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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