A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003496



Internal ID18746027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9929338..9954661hg38UCSC Ensembl
Innerchr4:9930962..9956285hg19UCSC Ensembl
Innerchr4:9540060..9565383hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3825324
hg1925324
hg1825324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3613422
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)nsv1003496
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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