A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357905



Internal ID22583574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129802889..129807022hg38UCSC Ensembl
chr11:129672784..129676917hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg384134
hg194134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925460
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357905
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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