A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416767



Internal ID21074320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128209796..128215443hg38UCSC Ensembl
chr7:127849849..127855496hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg385648
hg195648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416767
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