A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143870



Internal ID21438930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58350137..58350137hg38UCSC Ensembl
chr5:57645964..57645964hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628627
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143870
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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