A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101073



Internal ID21508661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23870992..23870992hg38UCSC Ensembl
chr18:21450956..21450956hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646104
Supporting Variants
SamplesNA20509
Known GenesLAMA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101073
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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