A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609315



Internal ID20982386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142833363..142833559hg38UCSC Ensembl
chr6:143154500..143154696hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140182
Samples
Known GenesHIVEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609315
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