A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022587



Internal ID19111805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137135135..137450828hg38UCSC Ensembl
Innerchr4:138056289..138371982hg19UCSC Ensembl
Innerchr4:138275739..138591432hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38315694
hg19315694
hg18315694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641124
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)nsv1022587
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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