A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293977



Internal ID20503195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71500153..71500153hg38UCSC Ensembl
chr3:71549304..71549304hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752699
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293977
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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