A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995744



Internal ID64601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45242076..45242228hg38UCSC Ensembl
chr7:45281675..45281827hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995744
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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