A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916676



Internal ID22691895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88881414..88881559hg38UCSC Ensembl
chr10:90641171..90641316hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366462
Samples
Known GenesSTAMBPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916676
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