A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018087



Internal ID19107304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164517686..164627459hg38UCSC Ensembl
Innerchr6:164938719..165048492hg19UCSC Ensembl
Innerchr6:164858709..164968482hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38109774
hg19109774
hg18109774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655394
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)nsv1018087
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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