A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358547



Internal ID21016100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155081001..155083900hg38UCSC Ensembl
chr3:154798790..154801689hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096395
Samples
Known GenesMME
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358547
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