A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063236



Internal ID21491514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229900689..229900782hg38UCSC Ensembl
chr1:230036436..230036529hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584004
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063236
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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