A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022118



Internal ID19111336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19138452..19478537hg38UCSC Ensembl
Innerchr7:19178075..19518160hg19UCSC Ensembl
Innerchr7:19144600..19484685hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38340086
hg19340086
hg18340086
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643240
Samples
Known GenesFERD3L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022118
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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