A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537082



Internal ID20910422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30193901..30277000hg38UCSC Ensembl
chr21:31566219..31649318hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3883100
hg1983100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072088
Samples
Known GenesCLDN8, LINC00307
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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