A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001832



Internal ID18744363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9810181..9895896hg38UCSC Ensembl
Innerchr4:9811805..9897520hg19UCSC Ensembl
Innerchr4:9420903..9506618hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3885716
hg1985716
hg1885716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5119n100
Supporting Variantsnssv3613420
Samples
Known GenesSLC2A9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001832
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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