A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414579



Internal ID22472449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71158113..71158113hg38UCSC Ensembl
chr3:71207264..71207264hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947685
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414579
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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