A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035932



Internal ID19125151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34565797hg38UCSC Ensembl
Innerchr15:34695310..34857998hg19UCSC Ensembl
Innerchr15:32482602..32645290hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38162689
hg19162689
hg18162689
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2559n100
Supporting Variantsnssv3548778, nssv3548789, nssv3548766, nssv3548771, nssv3548775, nssv3721727, nssv3548796, nssv3721722, nssv3721724, nssv3721728, nssv3548792, nssv3548790, nssv3548779, nssv3548791, nssv3721723, nssv3548793, nssv3548794, nssv3548783, nssv3548777, nssv3548786, nssv3548769, nssv3721726, nssv3548773, nssv3548774, nssv3548776, nssv3548785, nssv3548767, nssv3548780, nssv3721725, nssv3548772, nssv3721721, nssv3548770, nssv3548768, nssv3548787, nssv3548765, nssv3548782, nssv3548784, nssv3548781, nssv3548795, nssv3548788
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035932
Frequency
Sample Size11257
Observed Gain12
Observed Loss28
Observed Complex0
Frequencyn/a


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