A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364816



Internal ID22590485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130148942..130151603hg38UCSC Ensembl
chr10:131947206..131949867hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382662
hg192662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909621
Supporting Variants
Samples
Known GenesGLRX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364816
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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