A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17428757



Internal ID22486627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183445267..183479440hg38UCSC Ensembl
chr4:184366420..184400593hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3834174
hg1934174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898692
Supporting Variants
Samples
Known GenesCDKN2AIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17428757
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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