A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033211



Internal ID19122433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177706645..177956385hg38UCSC Ensembl
Innerchr5:177133646..177383386hg19UCSC Ensembl
Innerchr5:177066252..177315992hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38249741
hg19249741
hg18249741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649286
Samples
Known GenesFAM153A, LOC728554
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033211
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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