A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759800



Internal ID19058081
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 StatusS
Merged Variantsnsv1035680
Supporting Variants
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)nssv3759800
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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