A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142167



Internal ID341367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6171121..6185784hg38UCSC Ensembl
chr10:6213084..6227747hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3814664
hg1914664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028961
Samples
Known GenesPFKFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142167
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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