A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037229



Internal ID18779760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84192647..84402534hg38UCSC Ensembl
Innerchr15:84861399..84957232hg19UCSC Ensembl
Innerchr15:82652403..82748236hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38209888
hg1995834
hg1895834
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3554664, nssv3554660, nssv3554662, nssv3554663, nssv3554661
Samples
Known GenesGOLGA6L4, LOC388152, LOC440300, LOC642423
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037229
Frequency
Sample Size29084
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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