A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427501



Internal ID22485371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157421624..157423872hg38UCSC Ensembl
chr5:156848632..156850880hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382249
hg192249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901529
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427501
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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