A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381581



Internal ID21039134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31729462..31739762hg38UCSC Ensembl
chr5:31729569..31739869hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3810301
hg1910301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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