A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528912



Internal ID15109519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:12100657..12113107hg38UCSC Ensembl
Innerchr12:12253591..12266041hg19UCSC Ensembl
Innerchr12:12144858..12157308hg18UCSC Ensembl
Innerchr12:12144858..12157308hg17UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3812451
hg1912451
hg1812451
hg1712451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705597
Samples
Known GenesMIR1244-1, MIR1244-2, MIR1244-3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528912
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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