A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759828



Internal ID18711423
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 StatusS
Merged Variantsnsv1036145
Supporting Variants
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)nssv3759828
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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