A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022243



Internal ID19111461
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 StatusM
Merged Variantsdgv7542n100
Supporting Variantsnssv3690148
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)nsv1022243
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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