A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455476



Internal ID22513353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94174778..94186035hg38UCSC Ensembl
chr11:93907944..93919201hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3811258
hg1911258
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857139
Supporting Variants
Samples
Known GenesPANX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455476
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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