A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542594



Internal ID20915852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8805463..8806046hg38UCSC Ensembl
chr1:8865522..8866105hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251934
Samples
Known GenesRERE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542594
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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