A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616579



Internal ID20989650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35319004..35321376hg38UCSC Ensembl
chr7:35358614..35360986hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg382373
hg192373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153680
Samples
Known GenesLOC401324
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616579
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