A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381745



Internal ID21039298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7264025..7269328hg38UCSC Ensembl
chr5:7264138..7269441hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385304
hg195304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132163
Samples
Known GenesMIR4454
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381745
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