A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420309



Internal ID22478179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157906013..157907721hg38UCSC Ensembl
chr5:157333021..157334729hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381709
hg191709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420309
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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