A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607281



Internal ID20980352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2319956..2326527hg38UCSC Ensembl
chr7:2359591..2366162hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg386572
hg196572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607281
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