A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569930



Internal ID20943001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147998270..147998366hg38UCSC Ensembl
chr3:147716057..147716153hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569930
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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