A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690148



Internal ID18988429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39445501..39798681hg38UCSC Ensembl
Innerchr9:41475094..41943699hg19UCSC Ensembl
Innerchr9:41465094..41933699hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38353181
hg19468606
hg18468606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022243
Supporting Variants
Samples
Known GenesLOC653501, SPATA31A5, SPATA31A7, ZNF658B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690148
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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