A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010560



Internal ID19099777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18890947..18966711hg38UCSC Ensembl
Innerchr4:18892570..18968334hg19UCSC Ensembl
Innerchr4:18501668..18577432hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3875765
hg1975765
hg1875765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619870
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)nsv1010560
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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