A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036106



Internal ID19125325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28666612..28713634hg38UCSC Ensembl
Innerchr15:28911758..28958780hg19UCSC Ensembl
Innerchr15:26710799..26757821hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3847023
hg1947023
hg1847023
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3721476, nssv3721477, nssv3721478
Samples
Known GenesGOLGA8M, HERC2P9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036106
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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