A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549670



Internal ID20922831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205102054..205102585hg38UCSC Ensembl
chr1:205071182..205071713hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249961
Samples
Known GenesRBBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549670
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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