A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061334



Internal ID21491787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171292080..171292401hg38UCSC Ensembl
chr1:171261219..171261540hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567281
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061334
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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