A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977136



Internal ID22752071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46610553..46613141hg38UCSC Ensembl
chr2:46837692..46840280hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg382589
hg192589
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390462
Samples
Known GenesPIGF
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977136
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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