A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411001



Internal ID21068554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156658801..156665500hg38UCSC Ensembl
chr5:156085812..156092511hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5999n223
Supporting Variantsnssv18215900
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411001
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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