A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014301



Internal ID19103522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:115981501..116225600hg38UCSC Ensembl
Innerchr4:116902657..117146756hg19UCSC Ensembl
Innerchr4:117122106..117366205hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38244100
hg19244100
hg18244100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639330
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)nsv1014301
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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