A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036034



Internal ID18778565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34427582..34522329hg38UCSC Ensembl
Innerchr15:34719783..34814530hg19UCSC Ensembl
Innerchr15:32507075..32601822hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3894748
hg1994748
hg1894748
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2562n100
Supporting Variantsnssv3721825, nssv3548968, nssv3548970, nssv3721799, nssv3548966, nssv3548985, nssv3548978, nssv3721808, nssv3721809, nssv3548972, nssv3721818, nssv3548963, nssv3721801, nssv3721807, nssv3548964, nssv3721819, nssv3721814, nssv3721793, nssv3721815, nssv3548982, nssv3548979, nssv3548961, nssv3721806, nssv3721821, nssv3548962, nssv3721797, nssv3548980, nssv3548976, nssv3721822, nssv3548981, nssv3721791, nssv3548965, nssv3548959, nssv3721824, nssv3721817, nssv3721792, nssv3721803, nssv3548967, nssv3721813, nssv3721798, nssv3548969, nssv3721816, nssv3721805, nssv3721810, nssv3548960, nssv3721820, nssv3721800, nssv3721811, nssv3721804, nssv3548983, nssv3548977, nssv3721790, nssv3721812, nssv3721796, nssv3721794, nssv3548971, nssv3548975, nssv3548973, nssv3721795, nssv3548974, nssv3721823, nssv3721802, nssv3548984
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)nsv1036034
Frequency
Sample Size29084
Observed Gain3
Observed Loss60
Observed Complex0
Frequencyn/a


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