A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050015



Internal ID18792546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99970171..99994875hg38UCSC Ensembl
Innerchr15:100510376..100535080hg19UCSC Ensembl
Innerchr15:98327899..98352603hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3824705
hg1924705
hg1824705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555327
Samples
Known GenesADAMTS17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050015
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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