A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257014



Internal ID21400535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:91839529..92053704hg38UCSC Ensembl
chr2:92027555..92241730hg19UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38214176
hg19214176
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730191
Supporting Variants
SamplesNA19240
Known GenesACTR3BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257014
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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