A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657183



Internal ID18955464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79691200..79772559hg38UCSC Ensembl
Innerchr7:79320516..79401875hg19UCSC Ensembl
Innerchr7:79158452..79239811hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3881360
hg1981360
hg1881360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020043
Supporting Variants
Samples
Known GenesMIR548M
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657183
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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