A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144982



Internal ID344187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36076653..36094632hg38UCSC Ensembl
chr15:36368854..36386833hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3817980
hg1917980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144982
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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