A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756547



Internal ID20532407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61109123..61357029hg38UCSC Ensembl
chr6:61880166..62178590hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38247907
hg19298425
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273347
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756547
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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