A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544484



Internal ID20917722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31474032..31541035hg38UCSC Ensembl
chr21:32846345..32913348hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3867004
hg1967004
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206063
Samples
Known GenesTIAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544484
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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