A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145836



Internal ID21487275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65512041..65512041hg38UCSC Ensembl
chr5:64807868..64807868hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630914
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145836
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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