A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405147



Internal ID21062700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81506843..81507187hg38UCSC Ensembl
chr5:80802662..80803006hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132896
Samples
Known GenesSSBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405147
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