A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138064



Internal ID21469758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181343337..181343337hg38UCSC Ensembl
chr5:180770338..180770338hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633482
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138064
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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