A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521523



Internal ID21845882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8101936..8104165hg38UCSC Ensembl
chr1:8161996..8164225hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382230
hg192230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521523
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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