A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975305



Internal ID22750240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104322834..104604950hg38UCSC Ensembl
chr4:105243991..105526107hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38282117
hg19282117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419719
Samples
Known GenesCXXC4
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975305
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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