A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044164



Internal ID19133383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..22032488hg38UCSC Ensembl
Innerchr15:20532605..22320439hg19UCSC Ensembl
Innerchr15:18792619..19821803hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381705137
hg191787835
hg181029185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2213n100
Supporting Variantsnssv3536189
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044164
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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