A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363205



Internal ID21020758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149364882..149367286hg38UCSC Ensembl
chr3:149082669..149085073hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382405
hg192405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363205
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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