A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031806



Internal ID19121028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:129231705..129257175hg38UCSC Ensembl
Innerchr4:130152860..130178330hg19UCSC Ensembl
Innerchr4:130372310..130397780hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3825471
hg1925471
hg1825471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639440
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)nsv1031806
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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