A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214095



Internal ID22360847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39811724..39900829hg38UCSC Ensembl
Outerchr9:41956742..42045847hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3889106
hg1989106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282791
SamplesHG00512
Known GenesKGFLP2, LOC643648
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214095
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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