A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419038



Internal ID21076591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156901454..156907390hg38UCSC Ensembl
chr7:156694148..156700084hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385937
hg195937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419038
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