A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603513



Internal ID20976584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134092570..134093041hg38UCSC Ensembl
chr6:134413708..134414179hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603513
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