A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568941



Internal ID20942012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120593241..123536832hg38UCSC Ensembl
chr6:120914387..123857977hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382943592
hg192943591
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269236
Samples
Known GenesCLVS2, FABP7, GJA1, HSF2, PKIB, SERINC1, SMPDL3A, TBC1D32, TRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568941
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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