A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553232



Internal ID20926341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85101509..85102141hg38UCSC Ensembl
chr2:85328632..85329264hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3952n223
Supporting Variantsnssv18260898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553232
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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