A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018887



Internal ID19108104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93844167..94547463hg38UCSC Ensembl
Innerchr6:94553885..95257181hg19UCSC Ensembl
Innerchr6:94610606..95313902hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38703297
hg19703297
hg18703297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648984, nssv3751237
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)nsv1018887
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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