A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030666



Internal ID19119885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..106980hg38UCSC Ensembl
Innerchr5:15520..107095hg19UCSC Ensembl
Innerchr5:68520..160095hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3891461
hg1991576
hg1891576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5513n100
Supporting Variantsnssv3636523, nssv3636524
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030666
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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