A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398166



Internal ID21055719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:144059180..144104382hg38UCSC Ensembl
chr5:143438745..143483947hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3845203
hg1945203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398166
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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