A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039104



Internal ID19128323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74228254..74282994hg38UCSC Ensembl
Innerchr9:76843170..76897910hg19UCSC Ensembl
Innerchr9:76032990..76087730hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3854741
hg1954741
hg1854741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7679n100
Supporting Variantsnssv3759769
Samples
Known GenesMIR6130
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039104
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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