A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053327



Internal ID19142546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..20418941hg38UCSC Ensembl
Innerchr15:20532605..20624194hg19UCSC Ensembl
Innerchr15:18792619..18884208hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3891590
hg1991590
hg1891590
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2242n100
Supporting Variantsnssv3713717, nssv3536150, nssv3536152, nssv3536147, nssv3536149, nssv3536148, nssv3536145, nssv3536151, nssv3536146
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053327
Frequency
Sample Size11257
Observed Gain7
Observed Loss2
Observed Complex0
Frequencyn/a


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