A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571233



Internal ID20944304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39644885..39645743hg38UCSC Ensembl
chr4:39646505..39647363hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265174
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571233
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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