A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521675



Internal ID21846034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202867909..202867988hg38UCSC Ensembl
chr1:202837037..202837116hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982270
Supporting Variants
Samples
Known GenesLOC148709
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521675
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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