A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015594



Internal ID19104811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114781483..114804997hg38UCSC Ensembl
Innerchr5:114117180..114140694hg19UCSC Ensembl
Innerchr5:114145079..114168593hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3823515
hg1923515
hg1823515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746588, nssv3647080
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)nsv1015594
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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