A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538815



Internal ID20912129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:13328345..14263387hg38UCSC Ensembl
chr21:14700666..15635708hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38935043
hg19935043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069294
Samples
Known GenesANKRD20A11P, C21orf15, LIPI, MIR3156-3, MIR8069, POTED, RBM11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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