A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037455



Internal ID18779986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430589..34563605hg38UCSC Ensembl
Innerchr15:34722790..34855806hg19UCSC Ensembl
Innerchr15:32510082..32643098hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38133017
hg19133017
hg18133017
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2559n100
Supporting Variantsnssv3549669, nssv3549663, nssv3549667, nssv3721922, nssv3549665, nssv3549664, nssv3549668, nssv3721923, nssv3549670, nssv3549666
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)nsv1037455
Frequency
Sample Size29084
Observed Gain1
Observed Loss9
Observed Complex0
Frequencyn/a


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