A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375981



Internal ID22601650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76527105..76555034hg38UCSC Ensembl
chr15:76819446..76847375hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3827930
hg1927930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936921
Supporting Variants
Samples
Known GenesSCAPER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375981
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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