A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511082



Internal ID18809363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120917298..120942908hg38UCSC Ensembl
Innerchr10:122676810..122702421hg19UCSC Ensembl
Innerchr10:122666800..122692411hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3825611
hg1925612
hg1825612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041302
Supporting Variants
Samples
Known GenesMIR5694
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511082
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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