A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385935



Internal ID22443805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77649014..77649071hg38UCSC Ensembl
chr15:77941356..77941413hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935923
Supporting Variants
Samples
Known GenesLOC253044
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385935
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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