A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221528



Internal ID20788568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64504464..64505542hg38UCSC Ensembl
chr12:64898244..64899322hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589128
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221528
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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