A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596453



Internal ID20969524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:21355200..21355705hg38UCSC Ensembl
chr21:22727520..22728025hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254230
Samples
Known GenesNCAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596453
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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