A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452128



Internal ID21109681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89202450..89217738hg38UCSC Ensembl
chr10:90962207..90977495hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3815289
hg1915289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984947
Samples
Known GenesCH25H, LIPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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