A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907434



Internal ID22682643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171324044..171325704hg38UCSC Ensembl
chr3:171041833..171043493hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381661
hg191661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415398
Samples
Known GenesTNIK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907434
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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