A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131892



Internal ID21421196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158440304..158440304hg38UCSC Ensembl
chr5:157867312..157867312hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg384932
hg194932
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630857
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131892
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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