A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016955



Internal ID19106172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43565662..43931647hg38UCSC Ensembl
Innerchr8:43420805..43786790hg19UCSC Ensembl
Innerchr8:43539962..43905947hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38365986
hg19365986
hg18365986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7189n100
Supporting Variantsnssv3687297
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016955
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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