A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373429



Internal ID21030982
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 StatusM
Merged Variants
Supporting Variantsnssv18101482
Samples
Known GenesPRICKLE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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