A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050541



Internal ID18793072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68087284..68144258hg38UCSC Ensembl
Innerchr15:68379622..68436596hg19UCSC Ensembl
Innerchr15:66166676..66223650hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3856975
hg1956975
hg1856975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2615n100
Supporting Variantsnssv3553656
Samples
Known GenesPIAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050541
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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