A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385966



Internal ID21043519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:126146601..126150400hg38UCSC Ensembl
chr4:127067756..127071555hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5439n223
Supporting Variantsnssv18210281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385966
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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