A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142502



Internal ID341702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112216152..112216207hg38UCSC Ensembl
chr9:114978432..114978487hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026300
Samples
Known GenesMIR3134
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142502
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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