A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605002



Internal ID21797049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84854229..84854229hg38UCSC Ensembl
chr15:85397460..85397460hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095921
Supporting Variants
Samples
Known GenesALPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605002
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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