A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015486



Internal ID19104703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140867540..140881629hg38UCSC Ensembl
Innerchr7:140567340..140581429hg19UCSC Ensembl
Innerchr7:140213809..140227898hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3814090
hg1914090
hg1814090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664284
Samples
Known GenesBRAF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015486
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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