A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228722



Internal ID22370814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:58169474..58214283hg38UCSC Ensembl
Outerchr10:59929235..59974044hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3844810
hg1944810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14280567
SamplesHG00732
Known GenesIPMK
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228722
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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