A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528012



Internal ID15455305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149221163..149249548hg38UCSC Ensembl
Innerchr3:148938950..148967335hg19UCSC Ensembl
Innerchr3:150421640..150450025hg18UCSC Ensembl
Innerchr3:150421648..150450033hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3828386
hg1928386
hg1828386
hg1728386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704540
Samples
Known GenesCP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528012
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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