A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027281



Internal ID19116500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130041790..130084613hg38UCSC Ensembl
Innerchr4:130962945..131005768hg19UCSC Ensembl
Innerchr4:131182395..131225218hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3842824
hg1942824
hg1842824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5387n100
Supporting Variantsnssv3639444
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)nsv1027281
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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