A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400735



Internal ID21058288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180951401..181052900hg38UCSC Ensembl
chr5:180378401..180479900hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38101500
hg19101500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6032n223
Supporting Variantsnssv18215170
Samples
Known GenesBTNL3, BTNL9, MIR8089
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400735
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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