A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552453



Internal ID20925581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14206573..14207202hg38UCSC Ensembl
chr21:15578894..15579523hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069365
Samples
Known GenesLIPI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552453
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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