A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142085



Internal ID341285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94333076..94340552hg38UCSC Ensembl
chr9:97095358..97102834hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387477
hg197477
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv547n206
Supporting Variantsnssv17025759
Samples
Known GenesLOC100132077
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142085
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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