A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544241



Internal ID20917480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:83982468..83989660hg38UCSC Ensembl
chr1:84448151..84455343hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg387193
hg197193
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253909
Samples
Known GenesTTLL7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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