A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549508



Internal ID20922669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39373508..39380986hg38UCSC Ensembl
chr21:40745434..40752912hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg387479
hg197479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203961
Samples
Known GenesWRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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