A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403074



Internal ID21060627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126376433..126380028hg38UCSC Ensembl
chr5:125712125..125715720hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg383596
hg193596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123729
Samples
Known GenesGRAMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403074
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