A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142773



Internal ID341974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94308552..94318552hg38UCSC Ensembl
chr9:97070834..97080834hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025753
Samples
Known GenesNUTM2F
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142773
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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