A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154520



Internal ID22085025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96898097..96927058hg38UCSC Ensembl
Outerchr9:96896925..96943417hg38UCSC Ensembl
Innerchr9:99660379..99689340hg19UCSC Ensembl
Outerchr9:99659207..99705699hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3846493
hg1946493
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006673, nssv4006674, nssv4006672
Samples
Known GenesLOC441454, NUTM2G
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154520
Frequency
Sample Size131
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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