A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554084



Internal ID20927193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:13929519..14041247hg38UCSC Ensembl
chr21:15301840..15413568hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38111729
hg19111729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069348
Samples
Known GenesANKRD20A11P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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