A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878669



Internal ID22653635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35640580..35640688hg38UCSC Ensembl
chr1:36106181..36106289hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382630
Samples
Known GenesPSMB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878669
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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