A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034055



Internal ID19123277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171484847..171579324hg38UCSC Ensembl
Innerchr4:172405998..172500475hg19UCSC Ensembl
Innerchr4:172642573..172737050hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3894478
hg1994478
hg1894478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5475n100
Supporting Variantsnssv3744515, nssv3635431
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)nsv1034055
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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