A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258227



Internal ID20825267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55329993..55330256hg38UCSC Ensembl
chr2:55557129..55557392hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548368
Supporting Variants
Samples
Known GenesCCDC88A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258227
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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