A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371373



Internal ID22597042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75270339..75786969hg38UCSC Ensembl
chr15:75562680..76079310hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38516631
hg19516631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928357
Supporting Variants
Samples
Known GenesCOMMD4, CSPG4, DNM1P35, GOLGA6C, GOLGA6D, IMP3, MAN2C1, MIR4313, MIR631, NEIL1, ODF3L1, PTPN9, SIN3A, SNUPN, SNX33
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371373
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