A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596225



Internal ID20969296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70648034..70648881hg38UCSC Ensembl
chr18:68315270..68316117hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244766
Samples
Known GenesGTSCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596225
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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