A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574621



Internal ID20947692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69249581..69250964hg38UCSC Ensembl
chr5:68545408..68546791hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266999
Samples
Known GenesCDK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574621
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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