A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458426



Internal ID22516309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62361072..62383747hg38UCSC Ensembl
chr11:62128544..62151219hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3822676
hg1922676
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862841
Supporting Variants
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458426
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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