A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434709



Internal ID22492579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3734687..3734787hg38UCSC Ensembl
chr9:3734687..3734787hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920888
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434709
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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