A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968933



Internal ID22743868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20564516..20600677hg38UCSC Ensembl
chr1:20891009..20927170hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3836162
hg1936162
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366829
Samples
Known GenesCDA
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968933
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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