A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362049



Internal ID21019602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153038781..153110689hg38UCSC Ensembl
chr3:152756570..152828478hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3871909
hg1971909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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