A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553571



Internal ID20926681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99217675..99677499hg38UCSC Ensembl
chr2:99834138..100293961hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38459825
hg19459824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258840
Samples
Known GenesAFF3, EIF5B, LYG1, LYG2, REV1, TXNDC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553571
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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