A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029648



Internal ID87463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137222200..137237536hg38UCSC Ensembl
chr9:140116652..140131988hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3815337
hg1915337
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142030
Supporting Variants
Samples
Known GenesC9orf169, RNF224, SLC34A3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029648
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.110526


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