A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043306



Internal ID19132525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20235273..20373039hg38UCSC Ensembl
Innerchr15:20440526..20578292hg19UCSC Ensembl
Innerchr15:18700540..18838306hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38137767
hg19137767
hg18137767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2220n100
Supporting Variantsnssv3539407
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)nsv1043306
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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