A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026314



Internal ID19115531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:118178266..118196681hg38UCSC Ensembl
Innerchr5:117513961..117532376hg19UCSC Ensembl
Innerchr5:117541860..117560275hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3818416
hg1918416
hg1818416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647225
Samples
Known GenesLOC102467224
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026314
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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