A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537547



Internal ID20910882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152461479..152881493hg38UCSC Ensembl
chr1:152433955..152853969hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38420015
hg19420015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247042
Samples
Known GenesC1orf68, CRCT1, KPRP, LCE1A, LCE1B, LCE1C, LCE1D, LCE1E, LCE1F, LCE2A, LCE2B, LCE2C, LCE2D, LCE3A, LCE3B, LCE3C, LCE3D, LCE3E, LCE4A, LCE5A, LCE6A, SMCP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537547
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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