A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031688



Internal ID19120910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141178932..141213123hg38UCSC Ensembl
Innerchr4:142100086..142134277hg19UCSC Ensembl
Innerchr4:142319536..142353727hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3834192
hg1934192
hg1834192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641188
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)nsv1031688
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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