A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933248



Internal ID22894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71376262..71379537hg38UCSC Ensembl
chr3:71425413..71428688hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383276
hg193276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453422
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933248
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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