A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196880



Internal ID22346821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75674876..75676490hg38UCSC Ensembl
chr4:76600060..76601674hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg381615
hg191615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314302, nssv14314301
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196880
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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