A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452265



Internal ID22510138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73050942..73068644hg38UCSC Ensembl
chr11:72761987..72779689hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3817703
hg1917703
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851340
Supporting Variants
Samples
Known GenesFCHSD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452265
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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