A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046730



Internal ID19135949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53229838..53295755hg38UCSC Ensembl
Innerchr15:53522035..53587952hg19UCSC Ensembl
Innerchr15:51309327..51375244hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3865918
hg1965918
hg1865918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2599n100
Supporting Variantsnssv3552418, nssv3552417, nssv3552416
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)nsv1046730
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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