A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205984



Internal ID22354597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38978932..38980106hg38UCSC Ensembl
chr1:39444604..39445778hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381175
hg191175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362714, nssv14362715
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205984
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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