A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549419



Internal ID16336828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:238452566..238520752hg38UCSC Ensembl
Innerchr1:238615866..238684052hg19UCSC Ensembl
Innerchr1:236682489..236750675hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3868187
hg1968187
hg1868187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv738854
Samples
Known GenesLINC01139
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549419
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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