A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368995



Internal ID21026548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134280922..134283186hg38UCSC Ensembl
chr3:133999764..134002028hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg382265
hg192265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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