A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526060



Internal ID21850418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178979050..179006606hg38UCSC Ensembl
chr1:178948185..178975741hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3827557
hg1927557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981858
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526060
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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