A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047148



Internal ID19136367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85689221..85708592hg38UCSC Ensembl
Innerchr15:86232452..86251823hg19UCSC Ensembl
Innerchr15:84033456..84052827hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3819372
hg1919372
hg1819372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718148
Samples
Known GenesAKAP13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047148
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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