A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022502



Internal ID19111720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140847211..140877135hg38UCSC Ensembl
Innerchr7:140547011..140576935hg19UCSC Ensembl
Innerchr7:140193480..140223404hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3829925
hg1929925
hg1829925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6643n100
Supporting Variantsnssv3664277, nssv3664273, nssv3664275, nssv3664278, nssv3664276, nssv3664274, nssv3664280, nssv3752534, nssv3664279
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)nsv1022502
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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