A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589663



Internal ID20962734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8631163..8632044hg38UCSC Ensembl
chr18:8631161..8632042hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38882
hg19882
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3276n223
Supporting Variantsnssv18244872
Samples
Known GenesRAB12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589663
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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