A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547880



Internal ID20921080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30209816..30219549hg38UCSC Ensembl
chr21:31582134..31591867hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg389734
hg199734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072090
Samples
Known GenesCLDN8, LINC00307
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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