A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023229



Internal ID21932572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44364203..44857549hg38UCSC Ensembl
chr15:44656401..45149747hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38493347
hg19493347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604098
Samples
Known GenesB2M, CASC4, CTDSPL2, EIF3J, EIF3J-AS1, PATL2, SPG11, TRIM69
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023229
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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