A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596608



Internal ID20969679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37018725..37019226hg38UCSC Ensembl
chr21:38391025..38391526hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254717
Samples
Known GenesRIPPLY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596608
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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