A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555358



Internal ID18853639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101491141..101611170hg38UCSC Ensembl
Innerchr15:102031344..102151373hg19UCSC Ensembl
Innerchr15:99848867..99968896hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38120030
hg19120030
hg18120030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044722
Supporting Variants
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)nssv3555358
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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