A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926702



Internal ID22701929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119773993..119780302hg38UCSC Ensembl
chr10:121533505..121539814hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg386310
hg196310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360693
Samples
Known GenesINPP5F
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926702
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