A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225895



Internal ID22368890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:138310166..138325132hg38UCSC Ensembl
Outerchr7:137994911..138009877hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3814967
hg1914967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277802
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225895
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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