A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051221



Internal ID18793752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134316739..134432274hg38UCSC Ensembl
Innerchr9:137208585..137324120hg19UCSC Ensembl
Innerchr9:136348406..136463941hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38115536
hg19115536
hg18115536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7723n100
Supporting Variantsnssv3696426, nssv3696425
Samples
Known GenesMIR4669, RXRA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051221
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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