A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247171



Internal ID20814211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10234934..10236240hg38UCSC Ensembl
chr1:10294992..10296298hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381307
hg191307
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536476
Supporting Variants
Samples
Known GenesKIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247171
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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