A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108153



Internal ID22017386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14058325..14065317hg38UCSC Ensembl
chr7:14097950..14104942hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg386993
hg196993
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108153
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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