A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920964



Internal ID22696187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35354953..35384390hg38UCSC Ensembl
chr10:35643881..35673318hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3829438
hg1929438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351919
Samples
Known GenesCCNY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920964
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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