A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938972



Internal ID22714359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95301994..96435598hg38UCSC Ensembl
chr15:95845223..96978828hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381133605
hg191133606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388923
Samples
Known GenesLINC00924, LOC400456, MIR1469, NR2F2, NR2F2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938972
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