A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374503



Internal ID21032056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157555301..157559600hg38UCSC Ensembl
chr3:157273090..157277389hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096533
Samples
Known GenesC3orf55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374503
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