A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444622



Internal ID21102175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92665085..92670768hg38UCSC Ensembl
chr10:94424842..94430525hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg385684
hg195684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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