A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449460



Internal ID21107013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88401171..88552949hg38UCSC Ensembl
chr10:90160928..90312706hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38151779
hg19151779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv846n223
Supporting Variantsnssv17984870
Samples
Known GenesRNLS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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