A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14257925



Internal ID22280364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:70716329..70736275hg38UCSC Ensembl
Outerchr15:71008668..71028614hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3819947
hg1919947
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224152
Supporting Variants
SamplesNA19239
Known GenesUACA
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14257925
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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