A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408992



Internal ID21066545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41995870..41998080hg38UCSC Ensembl
chr6:41963608..41965818hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382211
hg192211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143352
Samples
Known GenesCCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408992
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