A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157394



Internal ID21454882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98508230..98508545hg38UCSC Ensembl
chr5:97843934..97844249hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567412
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157394
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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