A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053220



Internal ID19142439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381480..22209017hg38UCSC Ensembl
Innerchr15:20586733..22496968hg19UCSC Ensembl
Innerchr15:18846747..19998332hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381827538
hg191910236
hg181151586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2192n100
Supporting Variantsnssv3538730
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, 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)nsv1053220
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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