A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14262526



Internal ID22185049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:40642988..40659895hg38UCSC Ensembl
Outerchr19:41148893..41165800hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3816908
hg1916908
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215723
Supporting Variants
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14262526
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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