A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103847



Internal ID22013080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137648100..137648194hg38UCSC Ensembl
chr6:137969237..137969331hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103847
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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