A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101628



Internal ID22010862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71433704..71435501hg38UCSC Ensembl
chr4:72299421..72301218hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381798
hg191798
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540750
Samples
Known GenesSLC4A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101628
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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