A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575027



Internal ID20948098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169215818..169216905hg38UCSC Ensembl
chr4:170136969..170138056hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg381088
hg191088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264375
Samples
Known GenesSH3RF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575027
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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