A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198915



Internal ID22348580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28131507..28131997hg38UCSC Ensembl
chr1:28458018..28458508hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357502
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198915
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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