A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031854



Internal ID19121076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:131900850..131969174hg38UCSC Ensembl
Innerchr5:131236543..131304867hg19UCSC Ensembl
Innerchr5:131264442..131332766hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3868325
hg1968325
hg1868325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648116
Samples
Known GenesACSL6, LOC728637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031854
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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