A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664281



Internal ID18962562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140861022..140876722hg38UCSC Ensembl
Innerchr7:140560822..140576522hg19UCSC Ensembl
Innerchr7:140207291..140222991hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3815701
hg1915701
hg1815701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017485
Supporting Variants
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)nssv3664281
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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