A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046590



Internal ID19135809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101688342..102086306hg38UCSC Ensembl
Innerchr9:104450624..104848588hg19UCSC Ensembl
Innerchr9:103490445..103888409hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38397965
hg19397965
hg18397965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697577
Samples
Known GenesGRIN3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046590
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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