A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154510



Internal ID22085015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485135..69505361hg38UCSC Ensembl
Outerchr9:69483652..69512262hg38UCSC Ensembl
Innerchr9:72100051..72120277hg19UCSC Ensembl
Outerchr9:72098568..72127178hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3828611
hg1928611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv301n97
Supporting Variantsnssv4006658
Samples
Known GenesAPBA1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154510
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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