A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047996



Internal ID18790527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99842460..100054405hg38UCSC Ensembl
Innerchr15:100382665..100594610hg19UCSC Ensembl
Innerchr15:98200188..98412133hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38211946
hg19211946
hg18211946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2667n100
Supporting Variantsnssv3555314
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)nsv1047996
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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