A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597940



Internal ID20971011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:21590025..25090354hg38UCSC Ensembl
chr21:22962346..26462667hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383500330
hg193500322
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254238
Samples
Known GenesD21S2088E, LINC00308, LINC00317, LOC339622
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597940
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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