A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035508



Internal ID19124727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..20381218hg38UCSC Ensembl
Innerchr15:20284054..20586471hg19UCSC Ensembl
Innerchr15:18544068..18846485hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38302418
hg19302418
hg18302418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2197n100
Supporting Variantsnssv3540024, nssv3540023, nssv3540021, nssv3540020, nssv3540025, nssv3540022, nssv3540019
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)nsv1035508
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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