A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448916



Internal ID21106469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89808883..90278467hg38UCSC Ensembl
chr10:91568640..92038224hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38469585
hg19469585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984980
Samples
Known GenesLINC00865
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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