A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205658



Internal ID22354324
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14318039, nssv14318038
SamplesHG00731, HG00733
Known GenesVEGFC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205658
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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