A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029291



Internal ID19118510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179833785..180294653hg38UCSC Ensembl
Innerchr4:180754938..181215806hg19UCSC Ensembl
Innerchr4:180991932..181452800hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38460869
hg19460869
hg18460869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635568
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)nsv1029291
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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