A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468431



Internal ID22526320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94123180..94133101hg38UCSC Ensembl
chr11:93856346..93866267hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389922
hg199922
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848140
Supporting Variants
Samples
Known GenesPANX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468431
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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