A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018200



Internal ID19107417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140847211..140876722hg38UCSC Ensembl
Innerchr7:140547011..140576522hg19UCSC Ensembl
Innerchr7:140193480..140222991hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3829512
hg1929512
hg1829512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6643n100
Supporting Variantsnssv3664271, nssv3664272
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)nsv1018200
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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