A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604728



Internal ID20977799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50844499..50854896hg38UCSC Ensembl
chr7:50912196..50922593hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3810398
hg1910398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604728
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