A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419602



Internal ID22477472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15841532..15847618hg38UCSC Ensembl
chr4:15843155..15849241hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg386087
hg196087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906238
Supporting Variants
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419602
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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