A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438204



Internal ID22496074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93889334..93889916hg38UCSC Ensembl
chr7:93518646..93519228hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921466
Supporting Variants
Samples
Known GenesTFPI2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438204
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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