A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555296



Internal ID20928388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25688800..25774683hg38UCSC Ensembl
chr21:27061112..27146994hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3885884
hg1985883
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206012
Samples
Known GenesATP5J, GABPA, JAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555296
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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