A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046777



Internal ID98996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65756967..65758206hg38UCSC Ensembl
chr11:65524438..65525677hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046777
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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