A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036145



Internal ID18778676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130499187..130619919hg38UCSC Ensembl
Innerchr9:133374574..133495306hg19UCSC Ensembl
Innerchr9:132364395..132485127hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38120733
hg19120733
hg18120733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7718n100
Supporting Variantsnssv3759828
Samples
Known GenesASS1, FUBP3, LOC100272217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036145
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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