A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535755



Internal ID20909108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108732165..108732977hg38UCSC Ensembl
chr1:109274787..109275599hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247269
Samples
Known GenesFNDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535755
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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