A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539631



Internal ID20912927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16338661..16366087hg38UCSC Ensembl
chr21:17710982..17738408hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3827427
hg1927427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070869
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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