A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030271



Internal ID19119490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:145147630..145190494hg38UCSC Ensembl
Innerchr5:144527193..144570057hg19UCSC Ensembl
Innerchr5:144507386..144550250hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3842865
hg1942865
hg1842865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5816n100
Supporting Variantsnssv3648157, nssv3746648
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)nsv1030271
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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