A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534774



Internal ID21859129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154996961..154997098hg38UCSC Ensembl
chr1:154969437..154969574hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981392
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534774
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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