A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036091



Internal ID19125310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39407640..39457992hg38UCSC Ensembl
Innerchr15:39699841..39750193hg19UCSC Ensembl
Innerchr15:37487133..37537485hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3850353
hg1950353
hg1850353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2579n100
Supporting Variantsnssv3552249
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)nsv1036091
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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