A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387443



Internal ID21044996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13578401..13578800hg38UCSC Ensembl
chr5:13578510..13578909hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387443
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