A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370549



Internal ID21028102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164258361..164377319hg38UCSC Ensembl
chr3:163976149..164095107hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38118959
hg19118959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5067n223
Supporting Variantsnssv18095518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370549
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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