A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152013



Internal ID20719053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104761525..104761932hg38UCSC Ensembl
chr7:104401972..104402379hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611940
Supporting Variants
Samples
Known GenesLHFPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152013
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00138


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