A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557260



Internal ID20930331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120500293..120792681hg38UCSC Ensembl
chr4:121421448..121713836hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38292389
hg19292389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263624
Samples
Known GenesPRDM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557260
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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