A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101482



Internal ID20668522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64174799..64175449hg38UCSC Ensembl
chr3:64160475..64161125hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373429
Supporting Variants
Samples
Known GenesPRICKLE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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