A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514932



Internal ID22572891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96818228..96826634hg38UCSC Ensembl
chr9:99580510..99588916hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg388407
hg198407
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859625
Supporting Variants
Samples
Known GenesZNF782
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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