A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038806



Internal ID18781337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28933682..28965543hg38UCSC Ensembl
Innerchr15:29225885..29257746hg19UCSC Ensembl
Innerchr15:27013177..27045038hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3831862
hg1931862
hg1831862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545675
Samples
Known GenesAPBA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038806
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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