A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548845



Internal ID20922023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172986906..172987184hg38UCSC Ensembl
chr2:173851634..173851912hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256115
Samples
Known GenesRAPGEF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548845
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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