A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063085



Internal ID21510329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233513863..233513863hg38UCSC Ensembl
chr1:233649609..233649609hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624350
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063085
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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