A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460821



Internal ID22518704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75433622..75437508hg38UCSC Ensembl
chr11:75144667..75148553hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383887
hg193887
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851279
Supporting Variants
Samples
Known GenesGDPD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460821
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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