A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051208



Internal ID18793739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34508394hg38UCSC Ensembl
Innerchr15:34695310..34800595hg19UCSC Ensembl
Innerchr15:32482602..32587887hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38105286
hg19105286
hg18105286
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2558n100
Supporting Variantsnssv3547911, nssv3721665, nssv3547907, nssv3721676, nssv3547908, nssv3548653, nssv3721666, nssv3548656, nssv3548650, nssv3548657, nssv3548654, nssv3548651, nssv3547905, nssv3721673, nssv3547902, nssv3548658, nssv3721672, nssv3721678, nssv3721674, nssv3721668, nssv3721677, nssv3721670, nssv3548652, nssv3721669, nssv3721675, nssv3721671, nssv3721679, nssv3548655, nssv3547903, nssv3721667, nssv3547904, nssv3547909, nssv3547906, nssv3547910
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051208
Frequency
Sample Size29084
Observed Gain4
Observed Loss30
Observed Complex0
Frequencyn/a


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