A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611292



Internal ID20984363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145832201..145833200hg38UCSC Ensembl
chr6:146153337..146154336hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140978
Samples
Known GenesLOC100507557
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611292
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