A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015269



Internal ID18757803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140712664..140759021hg38UCSC Ensembl
Innerchr7:140412464..140458821hg19UCSC Ensembl
Innerchr7:140058933..140105290hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3846358
hg1946358
hg1846358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664264
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)nsv1015269
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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