A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068626



Internal ID20635666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14468345..14468987hg38UCSC Ensembl
chr21:15840666..15841308hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542696
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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