A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568369



Internal ID20941440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6997572..9925632hg38UCSC Ensembl
chr7:7037203..9965264hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg382928061
hg192928062
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275069
Samples
Known GenesC1GALT1, COL28A1, GLCCI1, ICA1, LOC100131257, LOC101927354, MIOS, NXPH1, PER4, RPA3, RPA3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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