A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379733



Internal ID22437603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97077134..97077134hg38UCSC Ensembl
chr15:97620364..97620364hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978353
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379733
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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