A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063557



Internal ID21506651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24026255..24029122hg38UCSC Ensembl
chr1:24352745..24355612hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382868
hg192868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567612
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063557
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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