A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730199



Internal ID21401010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76106270..76159672hg38UCSC Ensembl
chr6:76815987..76869389hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3853403
hg1953403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257808, nssv16257105, nssv16257016, nssv16256240
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730199
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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