A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514703



Internal ID22572662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88483534..88489808hg38UCSC Ensembl
chr9:91098449..91104723hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386275
hg196275
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852539
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514703
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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