A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439471



Internal ID21097024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:54165628..54169708hg38UCSC Ensembl
chr10:55925388..55929468hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384081
hg194081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980906
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439471
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