A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047060



Internal ID18789591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104042528..104089565hg38UCSC Ensembl
Innerchr9:106804809..106851846hg19UCSC Ensembl
Innerchr9:105844630..105891667hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3847038
hg1947038
hg1847038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7695n100
Supporting Variantsnssv3697617
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)nsv1047060
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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