A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998478



Internal ID19158014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28737542..28863751hg38UCSC Ensembl
Innerchr4:28739164..28865373hg19UCSC Ensembl
Innerchr4:28348262..28474471hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38126210
hg19126210
hg18126210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620628
Samples
Known GenesMIR4275
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998478
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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