A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997816



Internal ID66084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74970584..74978779hg38UCSC Ensembl
chr7:74384734..74392920hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg388196
hg198187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997816
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000948


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer