A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357497



Internal ID21015050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147695048..147695420hg38UCSC Ensembl
chr3:147412835..147413207hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095753
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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