A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419062



Internal ID22476932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157700334..157721679hg38UCSC Ensembl
chr4:158621486..158642831hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3821346
hg1921346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906491
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419062
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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