A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065660



Internal ID21463967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56983048..56983139hg38UCSC Ensembl
chr1:57448721..57448812hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575217
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065660
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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