A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358129



Internal ID21015682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31622261..31622770hg38UCSC Ensembl
chr3:31663753..31664262hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099343
Samples
Known GenesSTT3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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