A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544723



Internal ID20917960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:218322841..218330580hg38UCSC Ensembl
chr1:218496183..218503922hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg387740
hg197740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248649
Samples
Known GenesRRP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544723
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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