A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206037



Internal ID22354641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:35037459..35062489hg38UCSC Ensembl
Outerchr1:35503060..35528090hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3825031
hg1925031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253324
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206037
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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