A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046162



Internal ID19135381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20384895hg38UCSC Ensembl
Innerchr15:20216943..20590148hg19UCSC Ensembl
Innerchr15:18476957..18850162hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38373206
hg19373206
hg18373206
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2185n100
Supporting Variantsnssv3536924, nssv3536921, nssv3715753, nssv3536923, nssv3536925, nssv3536922, nssv3536926, nssv3536920, nssv3715752
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046162
Frequency
Sample Size11257
Observed Gain1
Observed Loss8
Observed Complex0
Frequencyn/a


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