A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040746



Internal ID19129965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38834534..39035489hg38UCSC Ensembl
Innerchr15:39126735..39327690hg19UCSC Ensembl
Innerchr15:36914027..37114982hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38200956
hg19200956
hg18200956
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552243
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)nsv1040746
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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