A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436271



Internal ID21093824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31736722..31746133hg38UCSC Ensembl
chr11:31758270..31767681hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg389412
hg199412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188496
Samples
Known GenesELP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436271
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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