A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067082



Internal ID21490934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87581448..87581553hg38UCSC Ensembl
chr1:88047131..88047236hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582888
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067082
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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