A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048628



Internal ID18791159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39585297..39647903hg38UCSC Ensembl
Innerchr15:39877498..39940104hg19UCSC Ensembl
Innerchr15:37664790..37727396hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3862607
hg1962607
hg1862607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552250
Samples
Known GenesFSIP1, THBS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048628
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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