A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674661



Internal ID18972942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154357539..154421800hg38UCSC Ensembl
Innerchr7:154054624..154118885hg19UCSC Ensembl
Innerchr7:153685557..153749818hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3864262
hg1964262
hg1864262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026784
Supporting Variants
Samples
Known GenesDPP6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674661
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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