A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140818



Internal ID340011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:190173260..190192575hg38UCSC Ensembl
chrUn_gl000228:112091..129120hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3819316
hg1917030
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16960751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140818
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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