A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101909



Internal ID20668949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27450708..27451263hg38UCSC Ensembl
chr3:27492199..27492754hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371543
Supporting Variants
Samples
Known GenesSLC4A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00137


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