A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414572



Internal ID21072125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150374196..150438419hg38UCSC Ensembl
chr5:149753759..149817982hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3864224
hg1964224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213286
Samples
Known GenesCD74, TCOF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414572
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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