A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362729



Internal ID21020282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154427590..154437945hg38UCSC Ensembl
chr3:154145379..154155734hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3810356
hg1910356
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209737
Samples
Known GenesGPR149
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362729
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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