A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463491



Internal ID22521377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66642442..66656780hg38UCSC Ensembl
chr11:66409913..66424251hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3814339
hg1914339
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852194
Supporting Variants
Samples
Known GenesRBM14-RBM4, RBM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463491
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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