A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018051



Internal ID19107268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78166779..78332080hg38UCSC Ensembl
Innerchr6:78876496..79041797hg19UCSC Ensembl
Innerchr6:78933215..79098516hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38165302
hg19165302
hg18165302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6024n100
Supporting Variantsnssv3659082
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)nsv1018051
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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