A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490682



Internal ID267933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97331437..97331514hg38UCSC Ensembl
chr9:100093719..100093796hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738510
Samples
Known GenesCCDC180, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490682
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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