A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3231756



Internal ID22372324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:90629341..90666451hg38UCSC Ensembl
Outerchr15:91172573..91209682hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382167
hg192167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14259472
SamplesNA19239
Known GenesCRTC3
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3231756
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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