A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038843



Internal ID18781374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34517875hg38UCSC Ensembl
Innerchr15:34695310..34810076hg19UCSC Ensembl
Innerchr15:32482602..32597368hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38114767
hg19114767
hg18114767
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2558n100
Supporting Variantsnssv3548660, nssv3548661, nssv3548662, nssv3548659, nssv3548663, nssv3721680
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)nsv1038843
Frequency
Sample Size29084
Observed Gain1
Observed Loss5
Observed Complex0
Frequencyn/a


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