A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519519



Internal ID15100126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9862074..9863802hg38UCSC Ensembl
Innerchr4:9863698..9865426hg19UCSC Ensembl
Innerchr4:9472796..9474524hg18UCSC Ensembl
Innerchr4:9539967..9541695hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381729
hg191729
hg181729
hg171729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683059, nssv656596, nssv687874, nssv694171, nssv692351
Samples
Known GenesSLC2A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519519
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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