A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561338



Internal ID20934409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42112895..42114992hg38UCSC Ensembl
chr7:42152494..42154591hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382098
hg192098
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275943
Samples
Known GenesGLI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561338
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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