A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222924



Internal ID22366845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6819497..6833468hg38UCSC Ensembl
Outerchr10:6861459..6875430hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3813972
hg1913972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14275004, nssv14275003
SamplesNA19238, HG00513
Known GenesLINC00707
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222924
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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