A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142676



Internal ID341877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96906000..96939000hg38UCSC Ensembl
chr9:99668282..99701282hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3833001
hg1933001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026854
Samples
Known GenesLOC441454, NUTM2G
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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