A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543019



Internal ID20916270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178357806..178358948hg38UCSC Ensembl
chr1:178326941..178328083hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247797
Samples
Known GenesRASAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543019
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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