A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512238



Internal ID22570191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21277406..21280307hg38UCSC Ensembl
chr9:21277405..21280306hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382902
hg192902
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849118
Supporting Variants
Samples
Known GenesIFNA22P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512238
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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