A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053335



Internal ID18795866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20235273..22472558hg38UCSC Ensembl
Innerchr15:20440526..22752697hg19UCSC Ensembl
Innerchr15:18700540..20304061hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382237286
hg192312172
hg181603522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2179n100
Supporting Variantsnssv3713611
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L1, GOLGA6L6, GOLGA8CP, GOLGA8DP, HERC2P3, LOC646214, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053335
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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