A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514766



Internal ID22572725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92806518..92810870hg38UCSC Ensembl
chr9:95568800..95573152hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384353
hg194353
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850167
Supporting Variants
Samples
Known GenesANKRD19P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514766
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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