A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039585



Internal ID18782116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34522329hg38UCSC Ensembl
Innerchr15:34695310..34814530hg19UCSC Ensembl
Innerchr15:32482602..32601822hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38119221
hg19119221
hg18119221
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2558n100
Supporting Variantsnssv3721691, nssv3548687, nssv3721693, nssv3548679, nssv3548670, nssv3548688, nssv3548684, nssv3548678, nssv3721683, nssv3721688, nssv3548676, nssv3548677, nssv3721684, nssv3721692, nssv3548674, nssv3721690, nssv3548682, nssv3548671, nssv3721686, nssv3548672, nssv3548673, nssv3548680, nssv3721689, nssv3548681, nssv3548686, nssv3548683, nssv3721687, nssv3548685, nssv3548669, nssv3548675, nssv3721685
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)nsv1039585
Frequency
Sample Size29084
Observed Gain4
Observed Loss27
Observed Complex0
Frequencyn/a


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