A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514710



Internal ID22572669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88613001..88616350hg38UCSC Ensembl
chr9:91227916..91231265hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383350
hg193350
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514710
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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