A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254539



Internal ID20821579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:147988601..147989595hg38UCSC Ensembl
chr2:148746170..148747164hg19UCSC Ensembl
Cytoband2q23.1
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541236
Supporting Variants
Samples
Known GenesORC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254539
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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