A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045597



Internal ID18788128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30227368..30807411hg38UCSC Ensembl
Innerchr15:30519571..31099614hg19UCSC Ensembl
Innerchr15:28306863..28886906hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38580044
hg19580044
hg18580044
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2496n100
Supporting Variantsnssv3546665
Samples
Known GenesARHGAP11B, CHRFAM7A, GOLGA8H, LOC100288637, LOC101059918, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045597
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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