A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027885



Internal ID18770416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19138927..19227274hg38UCSC Ensembl
Innerchr8:18996437..19084784hg19UCSC Ensembl
Innerchr8:19040717..19129064hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3888348
hg1988348
hg1888348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3684214
Samples
Known GenesLOC100128993
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027885
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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