A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287232



Internal ID20496450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143213606..143213663hg38UCSC Ensembl
chr8:144295481..144295538hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742379
Supporting Variants
Samples
Known GenesGPIHBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287232
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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