A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140415



Internal ID339608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149997327..149997697hg38UCSC Ensembl
chr5:149376890..149377260hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974752
Samples
Known GenesTIGD6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140415
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer