A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035680



Internal ID19124899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104152475..104177760hg38UCSC Ensembl
Innerchr9:106914756..106940041hg19UCSC Ensembl
Innerchr9:105954577..105979862hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3825286
hg1925286
hg1825286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759800
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)nsv1035680
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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