A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140361



Internal ID21489668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60520103..60520103hg38UCSC Ensembl
chr5:59815930..59815930hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg382157
hg192157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632146
Supporting Variants
SamplesNA18939
Known GenesPART1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140361
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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