A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204429



Internal ID22353279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:99765918..99838675hg38UCSC Ensembl
Outerchr6:100213794..100286551hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3872758
hg1972758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14274841
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204429
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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