A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255997



Internal ID20823037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195968213..195976091hg38UCSC Ensembl
chr2:196832937..196840815hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg387879
hg197879
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553927
Supporting Variants
Samples
Known GenesDNAH7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255997
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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