A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971924



Internal ID22746859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104909912..104911897hg38UCSC Ensembl
chr7:104550359..104552344hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381986
hg191986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436880
Samples
Known GenesLHFPL3-AS2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971924
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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