A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464324



Internal ID22522210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36601439..36616892hg38UCSC Ensembl
chr11:36622989..36638442hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3815454
hg1915454
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857303
Supporting Variants
Samples
Known GenesC11orf74
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464324
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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