A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064210



Internal ID21404990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24634837..24634837hg38UCSC Ensembl
chr1:24961328..24961328hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619153
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064210
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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