A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192205



Internal ID22342818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5847831..5848221hg38UCSC Ensembl
chr1:5907891..5908281hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14303896, nssv14303897
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192205
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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