A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410634



Internal ID22468504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71345733..71351423hg38UCSC Ensembl
chr3:71394884..71400574hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg385691
hg195691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899248
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410634
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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