A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528849



Internal ID15109456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149054135..149117654hg38UCSC Ensembl
Innerchr3:148771922..148835441hg19UCSC Ensembl
Innerchr3:150254612..150318131hg18UCSC Ensembl
Innerchr3:150254620..150318139hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3863520
hg1963520
hg1863520
hg1763520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705528
Samples
Known GenesHLTF, HLTF-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528849
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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