A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018145



Internal ID19107362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91618674..92241844hg38UCSC Ensembl
Innerchr6:92328392..92951562hg19UCSC Ensembl
Innerchr6:92385113..93008283hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38623171
hg19623171
hg18623171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3751234
Samples
Known GenesCASC6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018145
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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