A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061437



Internal ID21462532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180551..180885hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572831
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061437
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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