A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873156



Internal ID22648100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37363260..37368551hg38UCSC Ensembl
chr18:34943223..34948514hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg385292
hg195292
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477923
Samples
Known GenesCELF4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873156
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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