A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441903



Internal ID22499773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91866156..91866453hg38UCSC Ensembl
chr9:94628438..94628735hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921334
Supporting Variants
Samples
Known GenesROR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441903
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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