A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022691



Internal ID19111909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17585689..17636339hg38UCSC Ensembl
Innerchr9:17585687..17636337hg19UCSC Ensembl
Innerchr9:17575687..17626337hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3850651
hg1950651
hg1850651
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7466n100
Supporting Variantsnssv3755823
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022691
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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