A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418272



Internal ID22476142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132507392..132507392hg38UCSC Ensembl
chr5:131843084..131843084hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958537
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418272
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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