A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139448



Internal ID21443151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176430386..176430588hg38UCSC Ensembl
chr5:175857387..175857589hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570877
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139448
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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