A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411236



Internal ID21068789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40738656..40856599hg38UCSC Ensembl
chr6:40706395..40824338hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38117944
hg19117944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411236
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