A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15196786



Internal ID21335582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179650349..179650476hg38UCSC Ensembl
chr5:179077350..179077477hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928210
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15196786
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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