A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539035



Internal ID20912342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10234822..10236106hg38UCSC Ensembl
chr1:10294880..10296164hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381285
hg191285
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv44n223
Supporting Variantsnssv18247170
Samples
Known GenesKIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539035
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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