A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067060



Internal ID21453515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86985383..86985434hg38UCSC Ensembl
chr1:87451066..87451117hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575470
Supporting Variants
SamplesHG02011
Known GenesHS2ST1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067060
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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