A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596596



Internal ID20969667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14943216..15864165hg38UCSC Ensembl
chr21:16315537..17236484hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38920950
hg19920948
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254132
Samples
Known GenesNRIP1, USP25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596596
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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