A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432293



Internal ID22490163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69710239..69711706hg38UCSC Ensembl
chr9:72325155..72326622hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg381468
hg191468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913867
Supporting Variants
Samples
Known GenesPTAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432293
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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