A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230117



Internal ID20797157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35899101..35963900hg38UCSC Ensembl
chr9:35899098..35963897hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3864800
hg1964800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448354
Supporting Variants
Samples
Known GenesHRCT1, LINC00961, OR2S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230117
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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