A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547696



Internal ID20920897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14605588..14616703hg38UCSC Ensembl
chr21:15977909..15989024hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3811116
hg1911116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203764
Samples
Known GenesLOC388813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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