A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999227



Internal ID19158763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19947287..19973782hg38UCSC Ensembl
Innerchr4:19948910..19975405hg19UCSC Ensembl
Innerchr4:19558008..19584503hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3826496
hg1926496
hg1826496
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619883
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)nsv999227
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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