A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125422



Internal ID21462626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141825402..141825402hg38UCSC Ensembl
chr5:141204967..141204967hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630242
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125422
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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