A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445778



Internal ID22503648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91727045..91727170hg38UCSC Ensembl
chr9:94489327..94489452hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917325
Supporting Variants
Samples
Known GenesROR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445778
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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