A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357021



Internal ID21014574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16601801..16609300hg38UCSC Ensembl
chr3:16643308..16650807hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208542
Samples
Known GenesDAZL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357021
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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