A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465699



Internal ID22523588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43920557..43929724hg38UCSC Ensembl
chr11:43942107..43951274hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg389168
hg199168
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865348
Supporting Variants
Samples
Known GenesALKBH3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465699
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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