A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108500



Internal ID22017734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64403298..64515369hg38UCSC Ensembl
chr7:63863676..63975747hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38112072
hg19112072
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558055
Samples
Known GenesYWHAEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108500
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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