A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582241



Internal ID20955312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19538553..19538949hg38UCSC Ensembl
chr16:19549875..19550271hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2721n223
Supporting Variantsnssv18239182
Samples
Known GenesCCP110
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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