A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063361



Internal ID21441094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219941483..219941554hg38UCSC Ensembl
chr1:220114825..220114896hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575697
Supporting Variants
SamplesHG00732
Known GenesRNU5F-1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063361
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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