A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012283



Internal ID19101501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18434740..18476031hg38UCSC Ensembl
Innerchr4:18436363..18477654hg19UCSC Ensembl
Innerchr4:18045461..18086752hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3841292
hg1941292
hg1841292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619869
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012283
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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