A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417413



Internal ID22475283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18840383..18841479hg38UCSC Ensembl
chr4:18842006..18843102hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg381097
hg191097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417413
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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