A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618272



Internal ID20991343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142648627..142653247hg38UCSC Ensembl
chr6:142969764..142974384hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384621
hg194621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618272
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