A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369573



Internal ID21027126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128051201..128053500hg38UCSC Ensembl
chr3:127770044..127772343hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208484
Samples
Known GenesSEC61A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369573
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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