A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017243



Internal ID19106460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:22944235..22978405hg38UCSC Ensembl
Innerchr7:22983854..23018024hg19UCSC Ensembl
Innerchr7:22950379..22984549hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3834171
hg1934171
hg1834171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643278
Samples
Known GenesFAM126A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017243
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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