A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048250



Internal ID19137469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:86583057..86602905hg38UCSC Ensembl
Innerchr15:87126288..87146136hg19UCSC Ensembl
Innerchr15:84927292..84947140hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3819849
hg1919849
hg1819849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555096
Samples
Known GenesAGBL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048250
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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