A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386910



Internal ID22444780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85513776..85515966hg38UCSC Ensembl
chr15:86057007..86059197hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg382191
hg192191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929454
Supporting Variants
Samples
Known GenesAKAP13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386910
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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