A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461656



Internal ID22519541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123307755..123310418hg38UCSC Ensembl
chr11:123178463..123181126hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382664
hg192664
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866344
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461656
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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