A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540704



Internal ID20913994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241109712..241110710hg38UCSC Ensembl
chr1:241273012..241274010hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250127
Samples
Known GenesRGS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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