A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045887



Internal ID18788418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104059467..104090136hg38UCSC Ensembl
Innerchr9:106821748..106852417hg19UCSC Ensembl
Innerchr9:105861569..105892238hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3830670
hg1930670
hg1830670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697632
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)nsv1045887
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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