A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427520



Internal ID22485390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157883434..157883434hg38UCSC Ensembl
chr5:157310442..157310442hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950409
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427520
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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