A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596476



Internal ID20969547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17794810..17795548hg38UCSC Ensembl
chr21:19167127..19167865hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38739
hg19739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254179
Samples
Known GenesC21orf91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596476
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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