A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925673



Internal ID22700900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127937579..127937713hg38UCSC Ensembl
chr10:129735843..129735977hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350206
Samples
Known GenesPTPRE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925673
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