A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014360



Internal ID19103579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:13278..51612hg38UCSC Ensembl
Innerchr4:13278..51506hg19UCSC Ensembl
Innerchr4:3278..41506hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3838335
hg1938229
hg1838229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5052n100
Supporting Variantsnssv3615224, nssv3615225
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)nsv1014360
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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