A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463555



Internal ID22521441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20604690..20624314hg38UCSC Ensembl
chr11:20626236..20645860hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3819625
hg1919625
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864368
Supporting Variants
Samples
Known GenesSLC6A5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463555
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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