A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372749



Internal ID22598418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97298912..97356545hg38UCSC Ensembl
chr15:97842142..97899775hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3857634
hg1957634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372749
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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