A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574291



Internal ID20947362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70827288..70828741hg38UCSC Ensembl
chr4:71693005..71694458hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381454
hg191454
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265969
Samples
Known GenesGRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574291
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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