A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026995



Internal ID19116214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140861022..140877135hg38UCSC Ensembl
Innerchr7:140560822..140576935hg19UCSC Ensembl
Innerchr7:140207291..140223404hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3816114
hg1916114
hg1816114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6644n100
Supporting Variantsnssv3664282
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)nsv1026995
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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