A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041107



Internal ID19130326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:86850861..86910505hg38UCSC Ensembl
Innerchr15:87394092..87453736hg19UCSC Ensembl
Innerchr15:85195096..85254740hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3859645
hg1959645
hg1859645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718150
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)nsv1041107
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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