A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368466



Internal ID21026019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65188904..65195510hg38UCSC Ensembl
chr3:65174579..65181185hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg386607
hg196607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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