A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049884



Internal ID19139103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20368893hg38UCSC Ensembl
Innerchr15:20216943..20574146hg19UCSC Ensembl
Innerchr15:18476957..18834160hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38357204
hg19357204
hg18357204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2180n100
Supporting Variantsnssv3535728, nssv3535729
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)nsv1049884
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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