A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048655



Internal ID18791186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41686193..41757162hg38UCSC Ensembl
Innerchr15:41978391..42049360hg19UCSC Ensembl
Innerchr15:39765683..39836652hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3870970
hg1970970
hg1870970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552260
Samples
Known GenesMGA, MIR626
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048655
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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