A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015180



Internal ID18757715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:95798653..95950742hg38UCSC Ensembl
Innerchr5:95134357..95286446hg19UCSC Ensembl
Innerchr5:95160113..95312202hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38152090
hg19152090
hg18152090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639940
Samples
Known GenesC5orf27, ELL2, GLRX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015180
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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