A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019222



Internal ID18761756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6328242..6402856hg38UCSC Ensembl
Innerchr9:6328242..6402856hg19UCSC Ensembl
Innerchr9:6318242..6392856hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3874615
hg1974615
hg1874615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7387n100
Supporting Variantsnssv3689079, nssv3689080
Samples
Known GenesTPD52L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019222
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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