A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566949



Internal ID20940020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41335614..41336014hg38UCSC Ensembl
chr4:41337631..41338031hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264620
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566949
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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