A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063774



Internal ID21433530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23837095..23837095hg38UCSC Ensembl
chr1:24163585..24163585hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613720
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063774
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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