A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407152



Internal ID21064705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139347461..139348747hg38UCSC Ensembl
chr5:138683150..138684436hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg381287
hg191287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125405
Samples
Known GenesPAIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407152
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