A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032672



Internal ID18775206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9182297..9843781hg38UCSC Ensembl
Innerchr5:9182409..9843893hg19UCSC Ensembl
Innerchr5:9235409..9896893hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38661485
hg19661485
hg18661485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746434, nssv3746435
Samples
Known GenesLOC285692, SEMA5A, SNHG18, SNORD123, TAS2R1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032672
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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