A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581761



Internal ID20954832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59346753..59347052hg38UCSC Ensembl
chr18:57013985..57014284hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245389
Samples
Known GenesLMAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581761
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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