A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403408



Internal ID21060961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64733111..64760531hg38UCSC Ensembl
chr5:64028938..64056358hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3827421
hg1927421
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214094
Samples
Known GenesSREK1IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403408
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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