A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048913



Internal ID18791444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34379873..34454249hg38UCSC Ensembl
Innerchr15:34672074..34746450hg19UCSC Ensembl
Innerchr15:32459366..32533742hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3874377
hg1974377
hg1874377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2551n100
Supporting Variantsnssv3547883
Samples
Known GenesGOLGA8A, 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)nsv1048913
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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