A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023482



Internal ID19112699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:129816348..129862422hg38UCSC Ensembl
Innerchr4:130737503..130783577hg19UCSC Ensembl
Innerchr4:130956953..131003027hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3846075
hg1946075
hg1846075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639441
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)nsv1023482
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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