A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664286



Internal ID18615881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140916028..141046545hg38UCSC Ensembl
Innerchr7:140615828..140746345hg19UCSC Ensembl
Innerchr7:140262297..140392814hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38130518
hg19130518
hg18130518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030195
Supporting Variants
Samples
Known GenesBRAF, MRPS33
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3664286
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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