A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514327



Internal ID22572285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76506258..76509557hg38UCSC Ensembl
chr9:79121174..79124473hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854205
Supporting Variants
Samples
Known GenesGCNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514327
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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