A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976931



Internal ID22751866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101997955..101998669hg38UCSC Ensembl
chr7:101641235..101641949hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433148
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976931
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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