A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452334



Internal ID21109887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88755454..88797919hg38UCSC Ensembl
chr10:90515211..90557676hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3842466
hg1942466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197037
Samples
Known GenesLIPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452334
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer