A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538252



Internal ID20911573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10366207..10367312hg38UCSC Ensembl
chr1:10426265..10427370hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381106
hg191106
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247192
Samples
Known GenesKIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538252
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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