A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450785



Internal ID21108338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92319901..92321300hg38UCSC Ensembl
chr10:94079658..94081057hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985406
Samples
Known GenesMARCH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450785
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