A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366829



Internal ID22592498
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 StatusS
Merged Variantsnsv5968933
Supporting Variants
Samples
Known GenesCDA
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366829
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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