A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049156



Internal ID19138375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20372799hg38UCSC Ensembl
Innerchr15:20216943..20578052hg19UCSC Ensembl
Innerchr15:18476957..18838066hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38361110
hg19361110
hg18361110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2180n100
Supporting Variantsnssv3715732
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)nsv1049156
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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