A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479190



Internal ID22537092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6395117..6397116hg38UCSC Ensembl
chr18:6395116..6397115hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884401
Supporting Variants
Samples
Known GenesL3MBTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479190
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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