A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514756



Internal ID22572715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91693966..91696499hg38UCSC Ensembl
chr9:94456248..94458781hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382534
hg192534
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514756
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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