A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042872



Internal ID19132091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101494988..101599145hg38UCSC Ensembl
Innerchr15:102035191..102139348hg19UCSC Ensembl
Innerchr15:99852714..99956871hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38104158
hg19104158
hg18104158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2678n100
Supporting Variantsnssv3555365
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)nsv1042872
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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