A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378738



Internal ID21036291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12323501..12700400hg38UCSC Ensembl
chr5:12323613..12700512hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38376900
hg19376900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5643n223
Supporting Variantsnssv18123871
Samples
Known GenesCT49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378738
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