A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418569



Internal ID22476439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:95181982..95182045hg38UCSC Ensembl
chr4:96103133..96103196hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897134
Supporting Variants
Samples
Known GenesUNC5C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418569
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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