A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053108



Internal ID18795639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99837114..100060270hg38UCSC Ensembl
Innerchr15:100377319..100600475hg19UCSC Ensembl
Innerchr15:98194842..98417998hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38223157
hg19223157
hg18223157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2667n100
Supporting Variantsnssv3555311
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)nsv1053108
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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