A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512156



Internal ID22570108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19263294..19271654hg38UCSC Ensembl
chr9:19263292..19271652hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg388361
hg198361
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855673
Supporting Variants
Samples
Known GenesDENND4C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512156
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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