A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535177



Internal ID21859532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:146031200..146034068hg38UCSC Ensembl
chr1:145400932..145403801hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg382869
hg192870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981351
Supporting Variants
Samples
Known GenesLOC100288142, NBPF10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535177
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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