A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998838



Internal ID19158374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25500435..25515129hg38UCSC Ensembl
Innerchr4:25502057..25516751hg19UCSC Ensembl
Innerchr4:25111155..25125849hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3814695
hg1914695
hg1814695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620598
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)nsv998838
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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