A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430283



Internal ID22488153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35803099..35803401hg38UCSC Ensembl
chr9:35803096..35803398hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921225
Supporting Variants
Samples
Known GenesNPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430283
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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