A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582671



Internal ID20955742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58171518..58171873hg38UCSC Ensembl
chr16:58205422..58205777hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239334
Samples
Known GenesCSNK2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582671
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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