A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049619



Internal ID19138838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52703440..52749690hg38UCSC Ensembl
Innerchr15:52995637..53041887hg19UCSC Ensembl
Innerchr15:50782929..50829179hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3846251
hg1946251
hg1846251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2596n100
Supporting Variantsnssv3716726
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049619
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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