A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207977



Internal ID22356289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56962829..56963319hg38UCSC Ensembl
chr4:57828995..57829485hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312991
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207977
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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