A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018940



Internal ID19108157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10343376..10363463hg38UCSC Ensembl
Innerchr8:10200886..10220973hg19UCSC Ensembl
Innerchr8:10238296..10258383hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3820088
hg1920088
hg1820088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681717, nssv3681716
Samples
Known GenesMSRA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018940
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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