A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935351



Internal ID22710691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84853662..84853906hg38UCSC Ensembl
chr15:85396893..85397137hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375470
Samples
Known GenesALPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935351
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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