A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425039



Internal ID22482909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67930699..68011942hg38UCSC Ensembl
chr4:68796417..68877660hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3881244
hg1981244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902126
Supporting Variants
Samples
Known GenesTMPRSS11A, TMPRSS11GP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425039
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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