A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029363



Internal ID19118582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140867336..140894273hg38UCSC Ensembl
Innerchr7:140567136..140594073hg19UCSC Ensembl
Innerchr7:140213605..140240542hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3826938
hg1926938
hg1826938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664283
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)nsv1029363
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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