A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190803



Internal ID22341610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184234142..184234612hg38UCSC Ensembl
chr4:185155295..185155765hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14316813, nssv14316811, nssv14316809, nssv14316810, nssv14316812
SamplesHG00512, NA19239, HG00731, HG00732, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190803
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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