A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14318038



Internal ID22191123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176766589..176767124hg38UCSC Ensembl
chr4:177687743..177688278hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205658
Supporting Variants
SamplesHG00731
Known GenesVEGFC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14318038
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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