A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618321



Internal ID20991392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135262901..135349300hg38UCSC Ensembl
chr6:135584039..135670438hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3886400
hg1986400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139474
Samples
Known GenesAHI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618321
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