A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547140



Internal ID20920346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32043428..32098409hg38UCSC Ensembl
chr21:33415741..33470722hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3854982
hg1954982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206649
Samples
Known GenesLINC00159
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547140
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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