A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364073



Internal ID21021626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138053724..138084338hg38UCSC Ensembl
chr3:137772566..137803180hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3830615
hg1930615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209615
Samples
Known GenesDZIP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364073
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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