A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715781



Internal ID19014062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..22097038hg38UCSC Ensembl
Innerchr15:20216943..22384989hg19UCSC Ensembl
Innerchr15:18476957..19886353hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382085349
hg192168047
hg181409397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052894
Supporting Variants
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, 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)nssv3715781
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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