A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548018



Internal ID21872373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71113733..71113733hg38UCSC Ensembl
chr3:71162884..71162884hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067443
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548018
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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