A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549267



Internal ID15989990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:225891215..225947432hg38UCSC Ensembl
Innerchr1:226078915..226135132hg19UCSC Ensembl
Innerchr1:224145538..224201755hg18UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3856218
hg1956218
hg1856218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv737365
Samples
Known GenesLEFTY2, MIR6741, PYCR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549267
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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