A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064171



Internal ID21505126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24852249..24857534hg38UCSC Ensembl
chr1:25178740..25184025hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385286
hg195286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573724
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064171
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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