A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445962



Internal ID21103515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99859699..99915230hg38UCSC Ensembl
chr10:101619456..101674987hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3855532
hg1955532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985887
Samples
Known GenesDNMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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