A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044644



Internal ID97504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32095661..32140459hg38UCSC Ensembl
chr11:32117207..32162005hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3844799
hg1944799
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559539
Supporting Variants
Samples
Known GenesRCN1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044644
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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