A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203765



Internal ID22352725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:30114567..30114674hg38UCSC Ensembl
chr4:30116189..30116296hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14313341, nssv14313339, nssv14313340
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203765
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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