A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494727



Internal ID22552659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71345719..71351559hg38UCSC Ensembl
chr3:71394870..71400710hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg385841
hg195841
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836753
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494727
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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