A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415421



Internal ID22473291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151093366..151093366hg38UCSC Ensembl
chr5:150472927..150472927hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415421
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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