A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364576



Internal ID21022129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151766556..151768437hg38UCSC Ensembl
chr3:151484344..151486225hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381882
hg191882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096643
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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