A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542312



Internal ID20915576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10235251..10235746hg38UCSC Ensembl
chr1:10295309..10295804hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247172
Samples
Known GenesKIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542312
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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