A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139967



Internal ID339158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206152587..206160793hg38UCSC Ensembl
chr1:206180537..206188743hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg388207
hg198207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16895292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139967
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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