A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053635



Internal ID18796166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99814277..100059028hg38UCSC Ensembl
Innerchr15:100354482..100599233hg19UCSC Ensembl
Innerchr15:98172005..98416756hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38244752
hg19244752
hg18244752
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2667n100
Supporting Variantsnssv3555301, nssv3555302, nssv3555303, nssv3555304
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)nsv1053635
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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