A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529005



Internal ID15109612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:12101822..12259861hg38UCSC Ensembl
Innerchr12:12254756..12412795hg19UCSC Ensembl
Innerchr12:12146023..12304062hg18UCSC Ensembl
Innerchr12:12146023..12304062hg17UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38158040
hg19158040
hg18158040
hg17158040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705712
Samples
Known GenesLRP6, MIR1244-1, MIR1244-2, MIR1244-3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529005
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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