A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467398



Internal ID22525289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47144169..47151401hg38UCSC Ensembl
chr11:47165720..47172952hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg387233
hg197233
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866448
Supporting Variants
Samples
Known GenesC11orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467398
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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