A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563387



Internal ID20936458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108028029..108029866hg38UCSC Ensembl
chr7:107668474..107670311hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381838
hg191838
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273608
Samples
Known GenesLAMB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563387
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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