A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444784



Internal ID22502654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36323092..36323092hg38UCSC Ensembl
chr9:36323089..36323089hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444784
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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