A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547892



Internal ID20921092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14382601..14384300hg38UCSC Ensembl
chr21:15754922..15756621hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203761
Samples
Known GenesHSPA13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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