A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360633



Internal ID21018186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183145697..183156108hg38UCSC Ensembl
chr3:182863485..182873896hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3810412
hg1910412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098477
Samples
Known GenesLAMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360633
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer