A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258689



Internal ID20825729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:48446909..48447691hg38UCSC Ensembl
chr2:48674048..48674830hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548561
Supporting Variants
Samples
Known GenesPPP1R21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258689
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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