A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203644



Internal ID22352618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:15180915..15188309hg38UCSC Ensembl
Outerchr6:15181146..15188540hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg387395
hg197395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14274812
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203644
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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