A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828523



Internal ID22603458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167741919..167744394hg38UCSC Ensembl
chr1:167711156..167713631hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg382476
hg192476
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461875, nssv17456690
Samples
Known GenesMPZL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828523
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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