A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142627



Internal ID341828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2646620..3092107hg38UCSC Ensembl
chr10:2688812..3134299hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38445488
hg19445488
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv38n206
Supporting Variantsnssv17029355
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142627
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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