A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567319



Internal ID21759362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74211616..74213572hg38UCSC Ensembl
chr7:73625946..73627902hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381957
hg191957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012250
Supporting Variants
Samples
Known GenesLAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567319
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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