A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141187



Internal ID340382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14004916..14010916hg38UCSC Ensembl
chr4:14006540..14012540hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141187
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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