A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139950



Internal ID339141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224165884..224167078hg38UCSC Ensembl
chr1:224353586..224354780hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg381195
hg191195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139950
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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