A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249180



Internal ID20816220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10010562..10012272hg38UCSC Ensembl
chr1:10070620..10072330hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381711
hg191711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543044
Supporting Variants
Samples
Known GenesRBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249180
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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