A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832250



Internal ID22607185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23474271..23476697hg38UCSC Ensembl
chr2:23697141..23699567hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg382427
hg192427
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483373
Samples
Known GenesKLHL29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832250
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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