A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868870



Internal ID22643805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32067016..32098358hg38UCSC Ensembl
chr18:29646979..29678321hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3831343
hg1931343
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477893
Samples
Known GenesRNF125, RNF138
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868870
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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