A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405681



Internal ID21063234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75174175..75180684hg38UCSC Ensembl
chr5:74470000..74476509hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg386510
hg196510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216354
Samples
Known GenesANKRD31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405681
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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