A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050173



Internal ID18792704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20908759..22053726hg38UCSC Ensembl
Innerchr15:21114088..22341677hg19UCSC Ensembl
Innerchr15:19378713..19843041hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381144968
hg191227590
hg18464329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2347n100
Supporting Variantsnssv3541398
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, 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)nsv1050173
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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