A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037758



Internal ID19126977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37218138..37247606hg38UCSC Ensembl
Innerchr15:37510339..37539807hg19UCSC Ensembl
Innerchr15:35297631..35327099hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3829469
hg1929469
hg1829469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552236
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)nsv1037758
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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